FDA Inspection
LIFE CorporationLIFE Corporation – FDA Inspection, Dec 9, 2011
Record Details
This FDA Inspection record concerns LIFE Corporation, with an inspection on December 9, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- LIFE Corporation
- Inspection Date
- December 9, 2011
- Product Type
- Devices
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ID · ebb17faa-8b60-4b2a-bf31-6114e0b77b70
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 756787
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.40Lack of procedures, or not maintained
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
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Other FDA inspections of LIFE Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 7, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 18, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 10, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for LIFE Corporation
- FDA Inspection 1048141 - 2018-03-07
- FDA Inspection 918898 - 2015-03-18
- FDA Inspection 568402 - 2009-03-10
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