FDA Inspection 940730 — Microtek Medical, Inc.

Microtek Medical, Inc. — FEI 3000206154

The FDA completed an inspection of Microtek Medical, Inc. on Sep 2, 2015 in Jacksonville, FL. 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
Sep 2, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jacksonville, FL (United States)