FDA Inspection 1250876 — MAX HAUSER SUDDEUTSCHE CHIRURGIEMECHANIK GMBH

MAX HAUSER SUDDEUTSCHE CHIRURGIEMECHANIK GMBH — FEI 3008238512

The FDA completed an inspection of MAX HAUSER SUDDEUTSCHE CHIRURGIEMECHANIK GMBH on Sep 25, 2024 in Tuttlingen. 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)
End Date
Sep 25, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Tuttlingen (Germany)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation