FDA Inspection 709412 — Ledesma, Gilbert, M.D.
The FDA completed an inspection of Ledesma, Gilbert, M.D. on February 11, 2011 in Arlington, 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
- February 11, 2011
- Fiscal Year
- 2011
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- Arlington, TX (United States)
Additional Details
Clinical Investigator (CI)