Inspection report form

Report of results of every inspection made in pursuance of Construction (Health, Safety and Welfare) Regulations 

Name and address of person for whom inspection was carried out. 

Location and description of workpiace (inciuding any piant, equipment or materiais) inspected. 

Matters which give rise to any heaith and safety risks. 

Detaiis of any other action taken as a resuit of matters identified in 5 above. 

---

Completing formal reporting procedures. See Fig. 10-2 for an example of a sample inspection report form. 

CGA Pamphlet C-6 provides detailed instructions, and Appendix A provides a sample inspection report form. In general, all part of a cylinder (e.g., valves, neck rings, hoses, manifold, regulator, etc.) should be inspected, at a minimum, for ... 

For simple installations the sections do not insist on circuit diagrams but allow the relevant information to be provided in a schedule of the circuits fed from the distribution board(s). A typical example is given in Appendix 7 -Completion certificate and periodic inspection report form. 

When a roadside inspection is complete, whether it results in serious enough violations to warrant an Out-of-Service order or lesser violations that do not require immediate action or no violations at all, the driver should be issued a roadside inspection report form to forward to... 

The visual field inspection of derrick or mast and substructure procedure is recommended for use by operating personnel (or a designated representative) to the extent that its use satisfies conditions for which an inspection is intended. A sample report form for this inspection procedure can be found in API Standard 4F. Forms are also available from International Association of Drilling Contractors (lADC). 

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). 

Adverse events should be tabulated for easy inspection but the case report form should be available and all laboratory data such as blood coimts, renal function and liver function tests should be inspected closely The absence of obvious adverse events does not mean that all is well, and careful scrutiny of data by an experienced physician can often spot problems before they become troublesome. Not infrequently one or more volunteers become imwell during the course of a study, usually due to intercurrent viral infections, and decisions about postponement of study days and subject withdrawal follow-up can be made during these meetings. Data that are missing because of non-attendance of volunteers, for whatever reason, may lead to a delay in the study, with postponement of dose escalation imtil they have caught up. 

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. 

In addition to providing a form FDA-483, FDA investigators prepare an establishment inspection report (EIR), which is sent to FDA headquarters, which then evaluates the report and determines the corrective action, if any. The FDA then classifies the inspection as no action indicated, voluntary action indicated, or official action indicated. The EIR contains much greater detail than contained in the 483 and is not provided to the manufacturer until after the inspection is deemed closed. 

That done, the next step is not to do inference tests but, instead to inspect the raw data listings organized by variable, groups of variables, individual patients, and frequency distributions. Note observations or sets of data that are outliers by any large measure and track them as far back as necessary (all the way to the original case report forms if indicated). If the anomaly appears there, seek confirmation from the clinicians. The smaller the sample size, the more important this diligence becomes. 

Sponsors and monitors responsibilities in complying with GCPs are also subject to serious repercussions under 21CFR 312.58. FDA inspectors are allowed to examine sponsors files and the interventions of monitors site visits to assure that GCP compliance was executed. Case report forms and clinical results are subjected to the same scrutiny that are applied to the investigators responsibilities. If during an FDA inspection discrepancies are found in any form among the investigator, sponsor, and, when appropriate, the... 

Report development (e.g., training records, accident report forms, inspection forms)... 

An evaluation of the confinement functions in the HCF must consider the state of the confinement structures, and the potential flow and/or leakage paths that would result in dose consequences to either on-site or off-site personnel. Two outside evaluations of the seismic performance of HCF SSCs form the basis for this DBE analysis. The first, performed by Walla Engineering Ltd in December 1998, was an evaluation of the east shield wall of Zone 2A. This wall has the greatest potential for failure in a seismic event of ail of the basement concrete structural elements, since it is unrestrained at the top. The second evaluation is a qualitative assessment of several SSCs performed by Chavez-Grieves based on an on-sHe inspection, reported in memorandum format dated May 18,1999. 

Record Retention — You must retain a copy of all completed forms at your principal place of business, or where the vehicle is housed, for 12 months. Include all inspection reports in your individual vehicle maintenance files. 

Are drivers equipped with inspection aids and the necessary report forms ... 

---