FDA Inspection 882747 — Zopec Medical

Zopec Medical — FEI 3010266152

The FDA completed an inspection of Zopec Medical on Jun 9, 2014 in Crystal, MN. 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 9, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Crystal, MN (United States)