FDA Inspection
Recipharm Pharmaservices Private LimitedRecipharm Pharmaservices Private Limited – FDA Inspection, Dec 7, 2018
Record Details
This FDA Inspection record concerns Recipharm Pharmaservices Private Limited, with an inspection on December 7, 2018, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- December 7, 2018
- Product Type
- Human Drugs
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ID · 81f340a5-0e74-4b18-8dbb-cf65934bd357
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1075220
- FDA center
- Human Drugs
- Project area
- Generic Drug Evaluation
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 211.42(a)Buildings of Suitable Size, Construction, Location
- 21 CFR 211.42(c)Defined areas of adequate size for operations
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Other FDA inspections of Recipharm Pharmaservices Private Limited
8| Date | Classification | Office | Project area |
|---|---|---|---|
| March 22, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 13, 2020 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 1, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 11, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 14, 2017 | Not classified | Office of Inspections and Investigations |
Other documents for Recipharm Pharmaservices Private Limited
- FDA Inspection 1232473 - 2024-03-22
- FDA Inspection 1119410 - 2020-02-13
- FDA Inspection 1079034 - 2019-02-01
- FDA Inspection 1053644 - 2018-05-11
- FDA Inspection 1037690 - 2017-12-14
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