FDA Inspection 1066650 — Laborchemie Apolda GmbH

Laborchemie Apolda GmbH — FEI 3003585629

The FDA completed an inspection of Laborchemie Apolda GmbH on August 31, 2018 in Apolda. 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
August 31, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Apolda (Germany)