FDA Inspection 1241724 — Ana Leblanc, M.D.

Ana Leblanc, M.D. — FEI 3030523387

The FDA completed an inspection of Ana Leblanc, M.D. on May 24, 2024 in Porto. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
May 24, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Porto (Portugal)

Additional details

Clinical BA/BE

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