FDA Inspection 1300146 — Boehringer Ingelheim Hellas A.E.

Boehringer Ingelheim Hellas A.E. — FEI 3013350267

The FDA completed an inspection of Boehringer Ingelheim Hellas A.E. on Jun 4, 2024 in Koropi. 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
Jun 4, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Koropi (Greece)

Additional details

Mutual Recognition Agreement (MRA)

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