FDA Inspection 938900 — Amer Suleman
The FDA completed an inspection of Amer Suleman on July 13, 2015 in McKinney, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 13, 2015
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- McKinney, TX (United States)
Additional Details
Clinical Investigator (CI)