FDA Inspection 906511 — AMTRION GMBH (Formerly Haseke & Kroemker)
The FDA completed an inspection of AMTRION GMBH (Formerly Haseke & Kroemker) on December 11, 2014 in Porta Westfalica. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- December 11, 2014
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Porta Westfalica (Germany)