FDA Inspection 569481 — Charles F Bellows III, MD
The FDA completed an inspection of Charles F Bellows III, MD on Mar 16, 2009 in New Orleans, LA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Mar 16, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- New Orleans, LA (United States)
Additional Details
Clinical Investigator (CI)
Citations
| ID | CFR | Description |
|---|---|---|
| 2975 | 21 CFR 812.110(c) | Investigator did not supervise use of investigational device |
| 7391 | 21 CFR 50.25(a)(5) | Confidentiality, FDA inspection of records |