FDA Inspection
Life Technologies CorporationLife Technologies Corporation – FDA Inspection, Nov 3, 2016
Record Details
This FDA Inspection record concerns Life Technologies Corporation, with an inspection on November 3, 2016, issued by the Baltimore District Office, covering medical devices & rad health.
- Inspection Date
- November 3, 2016
- Product Type
- Medical Devices & Rad Health
- People
- Joshua D. Levin (Issuing Officer)
- Marc S. Neubauer (Issuing Officer)
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ID · 617baafb-2274-4298-9fa6-1f71c572abcf
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 991811
- FDA center
- Medical Devices & Rad Health
- Project area
- Project Evaluation: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.250(b)Sampling plans
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Life Technologies Corporation
5| Date | Classification | Office | Project area |
|---|---|---|---|
| December 16, 2024 | Not classified | Baltimore District Office | |
| June 14, 2021 | VAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| October 29, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| August 22, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 18, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Life Technologies Corporation
- FDA Inspection 1257089 - 2024-12-16
- FDA Inspection 1143829 - 2021-06-14
- FDA Inspection 902234 - 2014-10-29
- FDA Inspection 795459 - 2012-08-22
- FDA Inspection 725322 - 2011-05-18
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