FDA Compliance Program Guidance Manual. Section 4. Medical and radiological devices. Base Section (FY-92). Manual

Technical Report · Wed Jan 01 04:00:00 EST 1992

OSTI ID:5329133

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 (United States). Management Methods Branch
• OSTI ID: 5329133
• Report Number(s): PB-92-920999/XAB; FDA/OMO--92/23D
• Country of Publication: United States
• Language: English

Related Subjects

440100* -- Radiation Instrumentation
46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND TECHNOLOGY
COMPLIANCE
DOCUMENT TYPES
ELECTRONIC EQUIPMENT
EMERGENCY PLANS
EQUIPMENT
INSPECTION
MANUALS
MEDICINE
MICROWAVE EQUIPMENT
NATIONAL ORGANIZATIONS
NUCLEAR MEDICINE
PERFORMANCE TESTING
RADIOLOGY
STANDARDS
TESTING
US FDA
US HEW
US ORGANIZATIONS