FDA Inspection 1074891 — Instrumed GmbH

Instrumed GmbH — FEI 3007290840

The FDA completed an inspection of Instrumed GmbH on October 25, 2018 in Tuttlingen. 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
October 25, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tuttlingen (Germany)