FDA Inspection 684782 — Robert Booth
The FDA completed an inspection of Robert Booth on Oct 14, 2010 in Jacksonville, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Oct 14, 2010
- Fiscal Year
- 2011
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Jacksonville, FL (United States)
Additional Details
Clinical Investigator (CI)