FDA Inspection 1267183 — Maria Candela Etchegaray

Maria Candela Etchegaray — FEI 3033814158

The FDA completed an inspection of Maria Candela Etchegaray on Mar 31, 2025 in Buenos Aires. 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
Mar 31, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Buenos Aires (Argentina)

Additional details

Clinical Investigator (CI)

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