FDA Inspection 1029101 — Gilbert J. Martinez, MD

Gilbert J. Martinez, MD — FEI 3011080107

The FDA completed an inspection of Gilbert J. Martinez, MD on August 4, 2017 in Montclair, CA. 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
August 4, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Montclair, CA (United States)

Additional Details

Clinical Investigator (CI)