FDA Inspection 1080989 — Rachel L. Moore, M.D.
The FDA completed an inspection of Rachel L. Moore, M.D. on Feb 21, 2019 in Metairie, LA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 21, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Metairie, LA (United States)
Additional Details
Clinical Investigator (CI)