FDA Inspection 1258115 — KLS Martin SE & Co. KG

KLS Martin SE & Co. KG — FEI 3002807464

The FDA completed an inspection of KLS Martin SE & Co. KG on April 9, 2025 in Muhlheim An Der Donau. 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
April 9, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Muhlheim An Der Donau (Germany)