FDA Inspection
Promethean LifeSciences, Inc.Promethean LifeSciences, Inc. – FDA Inspection, Apr 28, 2009
Record Details
This FDA Inspection record concerns Promethean LifeSciences, Inc., with an inspection on April 28, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- April 28, 2009
- Product Type
- Biologics
View Company Profile
ID · 7a0b4c26-3772-4b58-8100-853f418170f7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 577659
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
4- 21 CFR 1271.260(e)Periodic review of temperatures
- 21 CFR 1271.270(a)Records maintained concurrently
- 21 CFR 1271.160(b)(1)Ensuring appropriate core requirements followed
- 21 CFR 1271.160(b)(2)Sharing of information (general)
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Other FDA inspections of Promethean LifeSciences, Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| February 18, 2026 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 9, 2022 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 28, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 7, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 11, 2015 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Promethean LifeSciences, Inc.
- FDA Inspection 1304480 - 2026-02-18
- FDA Inspection 1172008 - 2022-06-09
- FDA Inspection 1021850 - 2017-06-28
- FDA Inspection 962793 - 2016-03-07
- FDA Inspection 917223 - 2015-03-11
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