FDA Inspection
Life Technologies CorporationLife Technologies Corporation – FDA Inspection, Jan 20, 2015
Record Details
This FDA Inspection record concerns Life Technologies Corporation, with an inspection on January 20, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 20, 2015
- Product Type
- Devices
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ID · f6fc41dd-210c-4181-9c75-236248f40b54
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 911101
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
6- 21 CFR 803.50(a)(2)Individual Report of Malfunction
- 21 CFR 803.56Submission of Supplement to Individual Report Within One Month
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product control
- 21 CFR 806.10(c)(11)Domestic & foreign consignees
- 21 CFR 806.10(c)(9)Device number, identification
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Other FDA inspections of Life Technologies Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 5, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 14, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 11, 2008 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Life Technologies Corporation
- FDA Inspection 847614 - 2013-09-05
- FDA Inspection 744551 - 2011-09-14
- FDA Inspection 548712 - 2008-12-11
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