FDA Inspection 889779 — Buchler Gmbh

Buchler Gmbh — FEI 3002806608

The FDA completed an inspection of Buchler Gmbh on Mar 19, 2014 in Brunswick. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 19, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Brunswick (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.