| [Code of Federal Regulations] |
| [Title 21, Volume 8] |
| [Revised as of April 1, 2012] |
| [CITE: 21CFR820.60] |
|
|
|
CHAPTER I--FOOD AND DRUG ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES |
|
| SUBCHAPTER H--MEDICAL DEVICES |
|
PART 820 -- QUALITY SYSTEM REGULATION
Subpart F--Identification and Traceability
|
Sec. 820.60 Identification.
|
|
Each manufacturer shall establish and maintain procedures for identifying product during all stages of receipt, production, distribution, and installation to prevent mixups.
|
|