FDA Inspection 1010329 — SMT Schilling Metalltechnik GmbH

SMT Schilling Metalltechnik GmbH — FEI 3001026312

The FDA completed an inspection of SMT Schilling Metalltechnik GmbH on April 6, 2017 in Muhlheim An Der Donau. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 6, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Muhlheim An Der Donau (Germany)

Citations

IDCFRDescription
326221 CFR 820.250(a)Statistical techniques - Lack of or inadequate procedures