FDA Inspection 1113006 — Westmed, Inc.

Westmed, Inc. — FEI 1000374126

The FDA completed an inspection of Westmed, Inc. on December 11, 2019 in Tucson, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 11, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tucson, AZ (United States)

Citations

IDCFRDescription
337521 CFR 820.198(e)Records of complaint investigation
369621 CFR 820.100(b)Documentation