FDA Inspection
Robert J. Kreitman, MDRobert J. Kreitman, MD – FDA Inspection, Aug 28, 2015
Record Details
This FDA Inspection record concerns Robert J. Kreitman, MD, with an inspection on August 28, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Robert J. Kreitman, MD
- Inspection Date
- August 28, 2015
- Product Type
- Drugs
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ID · e2501174-117d-4b89-96c0-cbf5ad6dd7a9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 940561
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 312.60FD-1572, protocol compliance
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Other FDA inspections of Robert J. Kreitman, MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 3, 2022 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Robert J. Kreitman, MD
- FDA Inspection 1162932 - 2022-02-03
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