FDA Inspection 1160099 — K.D. Pharma Bexbach GmbH

K.D. Pharma Bexbach GmbH — FEI 3002655525

The FDA completed an inspection of K.D. Pharma Bexbach GmbH on May 14, 2020 in Bexbach. 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
May 14, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bexbach (Germany)

Additional Details

Mutual Recognition Agreement (MRA)