FDA Inspection 1089159 — Meribel Pharma Karlskoga AB

Meribel Pharma Karlskoga AB — FEI 3004713444

The FDA completed an inspection of Meribel Pharma Karlskoga AB on March 22, 2018 in Karlskoga. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 22, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Karlskoga (Sweden)

Additional Details

Mutual Recognition Agreement (MRA)