FDA Inspection 1026975 — Hevert Arzneimittel GmbH & Co. KG

Hevert Arzneimittel GmbH & Co. KG — FEI 3010165877

The FDA completed an inspection of Hevert Arzneimittel GmbH & Co. KG on September 29, 2017 in Nusbaum. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 29, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nusbaum (Germany)

Citations

IDCFRDescription
127421 CFR 211.68(a)Calibration/Inspection/Checking not done