FDA (Food and Drug Administration) Compliance Program Guidance Manual. Section 4. Medical and radiological devices. Irregular report

Technical Report · Sun Jan 01 04:00:00 EST 1984

OSTI ID:6402214

The FDA Compliance Program Guidance Manual provides a system for issuing and filing program plans and instructions directed to Food and Drug Administration Field operations for project implementation. Section IV provides those chapters of the Compliance Program Guidance Manual which pertain to the areas of medical and radiological devices. Some of the areas of coverage include laser and sunlamp standards inspections, compliance testing of various radiation-emitting products such as television receivers and microwave ovens, emergency response planning and policy, premarket approval and device manufacturers inspections, device problem reporting, sterilization of devices, and consumer education programs on medical and radiological devices.

• Research Organization: Food and Drug Administration, Rockville, MD (USA)
• OSTI ID: 6402214
• Report Number(s): PB-89-920900/XAB
• Country of Publication: United States
• Language: English

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550600 -- Medicine
560400* -- Other Environmental Pollutant Effects
62 RADIOLOGY AND NUCLEAR MEDICINE
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.
BIOMEDICAL RADIOGRAPHY
COMPLIANCE
CONSUMER PROTECTION
DIAGNOSTIC TECHNIQUES
DOCUMENT TYPES
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ELECTRONIC EQUIPMENT
EQUIPMENT
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