FDA Inspection 790329 — Oscor Inc.

Oscor Inc. — FEI 1035166

The FDA completed an inspection of Oscor Inc. on June 26, 2012 in Palm Harbor, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 26, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Palm Harbor, FL (United States)