FDA Inspection
Ronald E Pruitt, MDRonald E Pruitt, MD – FDA Inspection, Jul 1, 2016
Record Details
This FDA Inspection record concerns Ronald E Pruitt, MD, with an inspection on July 1, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Ronald E Pruitt, MD
- Inspection Date
- July 1, 2016
- Product Type
- Drugs
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ID · 348605da-22a9-444c-a248-85d94f143858
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 975226
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 312.60FD-1572, protocol compliance
- 21 CFR 312.62(a)Accountability records
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Other FDA inspections of Ronald E Pruitt, MD
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 11, 2014 | VAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| December 5, 2008 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
Other documents for Ronald E Pruitt, MD
- FDA Inspection 873833 - 2014-04-11
- FDA Inspection 553345 - 2008-12-05
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