FDA Warning Letter — GETSCH+HILLER MEDIZINTECHNIK GmbH

Case 644680 — FEI 3008911114

The FDA took a Warning Letter action against GETSCH+HILLER MEDIZINTECHNIK GmbH on December 27, 2022 (Tuttlingen, Germany). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
GETSCH+HILLER MEDIZINTECHNIK GmbH
Date
December 27, 2022
Fiscal Year
2023
Product Type
Devices
Center
CDRH
Location
Tuttlingen (Germany)