FDA Inspection 777589 — Microtek Medical, Inc.

Microtek Medical, Inc. — FEI 3000206154

The FDA completed an inspection of Microtek Medical, Inc. on Apr 12, 2012 in Jacksonville, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 12, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
383721 CFR 820.25(b)Training records
54621 CFR 820.75(a)Lack of or inadequate process validation