FDA Inspection 704474 — Buchler Gmbh

Buchler Gmbh — FEI 3002806608

The FDA completed an inspection of Buchler Gmbh on September 22, 2010 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
September 22, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brunswick (Germany)