FDA Inspection
Derek D. Muse, M.D., Clinical InvestigatorDerek D. Muse, M.D., Clinical Investigator – FDA Inspection, Jul 18, 2014
Record Details
This FDA Inspection record concerns Derek D. Muse, M.D., Clinical Investigator, with an inspection on July 18, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- July 18, 2014
- Product Type
- Drugs
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ID · d88ba993-c320-4142-a6a5-d9ef02596b12
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 896542
- 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 50.55(f)Documentation of permission by parents or guardian
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Derek D. Muse, M.D., Clinical Investigator
5| Date | Classification | Office | Project area |
|---|---|---|---|
| June 7, 2019 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| June 3, 2019 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| March 6, 2019 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| November 16, 2016 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| July 18, 2014 | VAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
Other documents for Derek D. Muse, M.D., Clinical Investigator
- FDA Inspection 1094879 - 2019-06-07
- FDA Inspection 1093583 - 2019-06-03
- FDA Inspection 1085336 - 2019-03-06
- FDA Inspection 998399 - 2016-11-16
- FDA Inspection 896759 - 2014-07-18
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