SPECIAL 510(k): Device Modification Review Memorandum To: THE FILE

First Page		Document Content
Validity Science Clinical research Food and Drug Administration Quality management Validation Labeling theory Packaging and labeling Verification and validation Technology Medicine Pharmaceutical industry		SPECIAL 510(k): Device Modification Review Memorandum To: THE FILE Add to Reading List Source URL: www.fda.gov Download Document from Source Website File Size: 94,45 KB Share Document on Facebook

	This is to certify that the Quality Management System of: Golden West Biologicals, IncCommerce Center Drive Temecula CACentral function listed above. See appendix for additional locations) DocID: 1vrli - View Document
	Fire Management Practices to Improve Air Quality Department of Agronomy DocID: 1vpIx - View Document
	EQUID Design Process Guidelines Requirements for ergonomic quality management in the design process for products and services Version 2.0 EQUID (Ergonomic Quality In Design) Technical Committee International Ergonomics A DocID: 1vn3X - View Document
	Certificate of Registration This certifies that the Quality Management System of Rogers Foam Corporation dba Rogers Foam Automotive Corporation 150 East Post Road DocID: 1vmVR - View Document
	Interagency Shoreline Management Consensus Document FINAL REPORT TO VIRGINIA COASTAL PROGRAM DEPARTMENT OF ENVIRONMENTAL QUALITY DocID: 1vmg9 - View Document