FDA Inspection 1032071 — Stryker Leibinger GmbH & Co. KG

Stryker Leibinger GmbH & Co. KG — FEI 3002821504

The FDA completed an inspection of Stryker Leibinger GmbH & Co. KG on July 27, 2017 in Freiburg Im Breisgau. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 27, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Freiburg Im Breisgau (Germany)