FDA Inspection 776993 — Meribel Pharma Karlskoga AB

Meribel Pharma Karlskoga AB — FEI 3004713444

The FDA completed an inspection of Meribel Pharma Karlskoga AB on Apr 5, 2012 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
Apr 5, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Karlskoga (Sweden)

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