FDA Inspection 1333758 — Meribel Pharma Karlskoga AB

Meribel Pharma Karlskoga AB — FEI 3004713444

The FDA completed an inspection of Meribel Pharma Karlskoga AB on Aug 29, 2025 in Karlskoga. 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
Aug 29, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Karlskoga (Sweden)

Additional Details

Mutual Recognition Agreement (MRA)

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