FDA Inspection 1025325 — Disch AG

Disch AG — FEI 3003840115

The FDA completed an inspection of Disch AG on September 8, 2017 in Othmarsingen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 8, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Othmarsingen (Switzerland)

Citations

IDCFRDescription
121321 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
139621 CFR 211.42(c)(2)Rejected Material Area
184421 CFR 211.84(d)(2)Establish reliability of supplier's C of A
202721 CFR 211.192Investigations of discrepancies, failures
440921 CFR 211.194(a)(4)Data secured in course of each test