| [Code of Federal Regulations] |
| [Title 21, Volume 8] |
| [Revised as of April 1, 2012] |
| [CITE: 21CFR820.130] |
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CHAPTER I--FOOD AND DRUG ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES |
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| SUBCHAPTER H--MEDICAL DEVICES |
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PART 820 -- QUALITY SYSTEM REGULATION
Subpart K--Labeling and Packaging Control
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Sec. 820.130 Device packaging.
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Each manufacturer shall ensure that device packaging and shipping containers are designed and constructed to protect the device from alteration or damage during the customary conditions of processing, storage, handling, and distribution.
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