Inspections reports

Of course, all the data displayed on a computer can be printed as like as an inspection report (protocol) (see Fig. 1,2). The report contains inspection results in short the LMA readings divided in four levels number of LF per a lot of the rope length, e.g. per 6 dia. 

As follow up, document the implementation of corrective actions taken by the toller. Keep this documentation with the initial inspection report that lists the deficiencies for which actions were taken. 

Are overdue inspections reported to the operations manager for his authorization for use of the equipment ... 

All correspondence, inspection reports, and other documents pertaining to the project, particularly those validating visits and inspections conducted by outside enforcement agencies, shall be kept in the project file. 

All other correspondence, inspection reports, approved contractor/ subcontractor invoices, and supporting documentation... 

Generate present inspection report with findings violations... 

The types of records needed to demonstrate adherence to requirements and standards as well as effective operation of the quality (ESH/PSM) management system are covered in this element. In addition to many of the quality records listed (e.g., inspection reports, audit reports, operational procedures, and drawings), ESH/PSM requirements might include training records, permits, hazard analyses, audit and other response plans, and accident/inci-dent investigation reports. 

This report evaluates recent performance of DGs and all DG vendors with the exception of Transamerica Delaval, Inc. (TDl), because of the emphasis already being given to TDI diesels in other studies. For the period 1980 through 1983 inclusive, BNL reviewed and evaluated DG failure data, DG vendor inspection reports, the TDI lessons learned as they related to the other vendors, and previous pertinent studies. The data sources used for DG failure analysis were LERs, 10 CFR 50.55E, Part 21, NPRDS, and EPRI document files. The DG failures were classified relative to the DG component that failed (e.g., main bearings, starting system). The failures were also categorized and analyzed by mode, manufacturer, and cause. Manufacturers with significant failures are identified in the report. 

Hazardous Substance Pressure Vessel Inspection Report... 

HAZARDOUS SUBSTANCE PRESSURE VESSEL INSPECTION REPORT... 

With each shipment of fresh catalyst, the catalyst suppliers typically mail refiners an inspection report that contains data on the catalyst s physical and chemical properties. This data is valuable and should be monitored closely to ensure that the catalyst received meets the agreed specifications. A number of refiners independently analyze random samples of the fresh catalyst to confirm the reported properties. In addition, quarterly review of the fresh catalyst properties with the catalyst vendor will ensure that the control targets are being achieved. 

For example, a catalyst with a MAT number of 70 vol% and a 3.0 wt% coke yield will have a dynamic activity of 0.78. However, another catalyst with a MAT conversion of 68 vol% and 2.5 wt% coke yield will have a dynamic activity of 0.85. This could indicate that in a commercial unit the 68 MAT catalyst could outperform the 70 MAT catalyst, due to its higher dynamic activity. Some catalyst vendors ha% c begun reporting dynamic activity data as part of their E-cat inspection reports. The reported dynamic activity data can vary significantly from one test to another, mainly due to the differences in feedstock quality between MAT and actual commercial application. In addition, the coke yield, as calculated by the MAT procedure, is not very accurate and small changes in this calculation can affect the dynamic activity appreciably. 

Name(s) Signatures(s) Organlsation(s) Date Distribution of Report The inspection report should be signed and dated by the inspector(s)/assessors having participated in the inspection. 

If the test facility claims to be GLP-compliant but is located in a country where there is no authorised body responsible for GLP monitoring, i.e., a national GLP compliance program, the Study Director needs to be assured that the facility (including the archive, if used) does operate in compliance with GLP principles. This can be achieved by conducting a pre-study QA test site inspection or by a review of documentary evidence, e.g., notice of adverse findings and subsequent responses, or Establishment Inspection reports. The Study Director should ideally discuss the above with QA personnel and send copies of any documentary evidence used to the Quality Assurance Unit (QAU) for inclusion in the QA multi-site study file. 

Procurement Fabrication Construction vendor and fabrication documents inspection reports field change documents vendor data on equipment as built data What-If, Checklist... 

After inspection, the inspector prepares a detailed Establishment Inspection Report (EIR). This is the FDA s primary record for the inspection. Time is given to the manufacturer to respond to the deficiencies found and recorded on Form FDA-483. Failure to comply with satisfactory resolution of the deficiencies found will result in the FDA sending out a Warning Letter notifying the manufacturer to comply. If the manufacturer is unable to resolve the deficiency after the deadline set by the FDA, the FDA may proceed to prosecute the manufacturer with an injunction. The injunction is a court order called Consent Decree, and the manufacturer may be required to cease operations until the problem is rectified (see Exhibit 10.4). 

Establishment Inspection Report Establishment License Application enzyme linked immunosorbent assay European Medicines Agency Environmental Protection Agency European Public Assessment Report end of production cell bank erythropoietin... 

All foam systems should be thoroughly inspected and checked for proper operation at least annually. The inspection should include performance evaluation of the foam concentrate or premix solution quantity or both. Test results that deviate more than 10% from those recorded in acceptance testing should be discussed immediately with the manufacturer. The inspection report should be documented with any deficiencies or recommendations included. Foam system inspections should include ... 

As part of the inspection report the QA persoimel specifies the inspection types and inspected phases and coirfirms that the final report reflects the raw data. 

Following inspection, an inspection report shall be prepared. It must be made available to the sponsor while safeguarding confidential aspects. It may be made available to the other Member States, to the Ethics Committee and to the Agency, at their reasoned request. 

The Team Biologics report is known as an Establishment Inspection Report, which consists of a list of observations recorded on a Form 483. In the Findings section, both products and processes are discussed and various processes are rated. Inspections of both products and the establishment focus on systematic evaluation of quality. Inspection Reports may recommend warning letters, notice of intent to revoke licenses, or civil or criminal legal action. 

After completion of visual inspection by manufacturing, QAI will perform (a) the review of printout of cold leak test carried out by production and (b) the visual inspection. See SOP (provide number). He gives the release for packing if the results are satisfactory. QAI will fill the optical inspection report attachment no. 1700.30(G) and 1700.30(H) for each batch optically inspected and for leakage. When packaging of the batch starts, the production supervisor will request the area QAI for line clearance. The QAI will check the area and countersign the line clearance given by the supervisor. See attachment no. 1700.30(B). 

Attachment No. 1700.30(H) OPTICAL INSPECTION REPORT IN-PROCESS CONTROL... 

When action level excursions or frequent alert excursions are identified, a corrective action program, resolution deadline, and preventive plan shall be implemented. Risk analysis shall be performed to determine the probability of one or more causes of errors occurring, as well as to identify the potential consequences of excursions. (See attachment nos. 1700.80(1), 1700.80(J), and 1700.80(K), and 1700.80(L) for excursion of air, surface, personnel, and visual inspection report during the visit to plant by the microbiologist responsible.)... 

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