FDA Inspection
Pharmaceutical Manufacturing Research Services, Inc (PMRS)Pharmaceutical Manufacturing Research Services, Inc (PMRS) – FDA Inspection, May 25, 2017
Record Details
This FDA Inspection record concerns Pharmaceutical Manufacturing Research Services, Inc (PMRS), with an inspection on May 25, 2017, issued by the Philadelphia District Office, covering human drugs.
- Inspection Date
- May 25, 2017
- Product Type
- Human Drugs
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ID · 27adefd8-3e92-4a3e-953d-cccdbd5e7829
Inspection Facts
- Inspection number
- 1015444
- FDA center
- Human Drugs
- Project area
- New Drug Evaluation
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 211.160(b)(4)Establishment of calibration procedures
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Other FDA inspections of Pharmaceutical Manufacturing Research Services, Inc (PMRS)
7| Date | Classification | Office | Project area |
|---|---|---|---|
| May 1, 2026 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 13, 2023 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 2, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 20, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 28, 2011 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Pharmaceutical Manufacturing Research Services, Inc (PMRS)
- FDA Inspection 1317554 - 2026-05-01
- FDA Inspection 1204311 - 2023-04-13
- FDA Inspection 994047 - 2016-12-02
- FDA Inspection 910560 - 2015-01-20
- FDA Inspection 736925 - 2011-07-28
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