FDA Inspection 1059880 — MICROTEK MEDICAL LLC

MICROTEK MEDICAL LLC — FEI 3005425620

The FDA completed an inspection of MICROTEK MEDICAL LLC on Jun 15, 2018 in Tyler, TX. 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 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tyler, TX (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.