FDA Inspection 1060993 — Omnitech Systems, Inc.

Omnitech Systems, Inc. — FEI 1000518605

The FDA completed an inspection of Omnitech Systems, Inc. on Jun 13, 2018 in Valparaiso, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 13, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Valparaiso, IN (United States)