FDA Inspection 1105834 — Buchler Gmbh

Buchler Gmbh — FEI 3002806608

The FDA completed an inspection of Buchler Gmbh on August 15, 2019 in Brunswick. 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 15, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brunswick (Germany)