FDA Inspection 1089159 — Meribel Pharma Karlskoga AB

Meribel Pharma Karlskoga AB — FEI 3004713444

The FDA completed an inspection of Meribel Pharma Karlskoga AB on Mar 22, 2018 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
Mar 22, 2018
Fiscal Year
2018
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.