FDA Inspection 1250211 — Maria Teresa Bourlon De Los Rios, M.D.

Maria Teresa Bourlon De Los Rios, M.D. — FEI 3031026737

The FDA completed an inspection of Maria Teresa Bourlon De Los Rios, M.D. on Sep 10, 2024 in Pueblo Nextlalpan. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 10, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Pueblo Nextlalpan (Mexico)

Additional Details

Clinical BA/BE