FDA Inspection 1340040 — Antonio Manuel Garrido Hermosilla, M.D.

Antonio Manuel Garrido Hermosilla, M.D. — FEI 3044760911

The FDA completed an inspection of Antonio Manuel Garrido Hermosilla, M.D. on Sep 18, 2026 in Sevilla. 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 18, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Sevilla (Spain)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.