FDA Inspection
Reproductive Gynecology LaboratoriesReproductive Gynecology Laboratories – FDA Inspection, Jan 15, 2013
Record Details
This FDA Inspection record concerns Reproductive Gynecology Laboratories, with an inspection on January 15, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- January 15, 2013
- Product Type
- Biologics
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ID · 570f29e4-8fe0-4e78-8454-1e325a7ee1e7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 813223
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
2- 21 CFR 1271.55(d)(2)Accurate, indelible, legible
- 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures
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Other FDA inspections of Reproductive Gynecology Laboratories
6| Date | Classification | Office | Project area |
|---|---|---|---|
| April 7, 2026 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| January 10, 2023 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| November 7, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| November 28, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| November 13, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Reproductive Gynecology Laboratories
- FDA Inspection 1312310 - 2026-04-07
- FDA Inspection 1194799 - 2023-01-10
- FDA Inspection 1110089 - 2019-11-07
- FDA Inspection 1032534 - 2017-11-28
- FDA Inspection 903327 - 2014-11-13
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