FDA Inspection
Westchester IVFWestchester IVF – FDA Inspection, Jun 12, 2013
Record Details
This FDA Inspection record concerns Westchester IVF, with an inspection on June 12, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Company
- Westchester IVF
- Inspection Date
- June 12, 2013
- Product Type
- Biologics
View Company Profile
ID · e267a6e5-9e44-4881-92ac-37e123c8d94e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 838589
- 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)Procedures for all other requirements
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Other FDA inspections of Westchester IVF
6| Date | Classification | Office | Project area |
|---|---|---|---|
| March 9, 2026 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| October 27, 2022 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 29, 2019 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 12, 2016 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| February 19, 2015 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Westchester IVF
- FDA Inspection 1310364 - 2026-03-09
- FDA Inspection 1183798 - 2022-10-27
- FDA Inspection 1085714 - 2019-03-29
- FDA Inspection 984424 - 2016-09-12
- FDA Inspection 918290 - 2015-02-19
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