FDA Inspection 884755 — Westmed, Inc.

Westmed, Inc. — FEI 1000374126

The FDA completed an inspection of Westmed, Inc. on June 18, 2014 in Tucson, AZ. 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 18, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Tucson, AZ (United States)