FDA Inspection
Zeid Kayali, M.D.Zeid Kayali, M.D. – FDA Inspection, Dec 21, 2017
Record Details
This FDA Inspection record concerns Zeid Kayali, M.D., with an inspection on December 21, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · b23fa479-7f75-415a-aaa7-5e95d1af73fd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1035889
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 312.62(b)Case history records- inadequate or inadequate
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Other FDA inspections of Zeid Kayali, M.D.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 24, 2018 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Zeid Kayali, M.D.
- FDA Inspection 1058474 - 2018-05-24
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