FDA Inspection 1099007 — Andrew R. Gould, M.D.
The FDA completed an inspection of Andrew R. Gould, M.D. on Aug 8, 2019 in Louisville, KY. 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). 1 citation was issued during this inspection. Product area: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 8, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Louisville, KY (United States)
Additional details
Clinical Investigator (CI)
Citations
| ID | CFR | Description |
|---|---|---|
| 2969 | 21 CFR 812.100 | No investigator protection - subject rights, safety, welfare |