FDA Inspection 1135782 — Quasaar GmbH

Quasaar GmbH — FEI 3014297892

The FDA completed an inspection of Quasaar GmbH on November 5, 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
November 5, 2020
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bexbach (Germany)

Additional Details

Mutual Recognition Agreement (MRA)