FDA Inspection
Multani, Gurmeet S., MDMultani, Gurmeet S., MD – FDA Inspection, Jan 29, 2013
Record Details
This FDA Inspection record concerns Multani, Gurmeet S., MD, with an inspection on January 29, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Multani, Gurmeet S., MD
- Inspection Date
- January 29, 2013
- Product Type
- Drugs
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ID · 5e6a2cc2-a733-4c62-9250-bbb1490fd156
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 816563
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 312.60FD-1572, protocol compliance
- 21 CFR 312.62(b)Case history records- inadequate or inadequate
- 21 CFR 312.64(b)Safety reports
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Other FDA inspections of Multani, Gurmeet S., MD
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 7, 2011 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Multani, Gurmeet S., MD
- FDA Inspection 709715 - 2011-01-07
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