FDA Inspection 1087893 — Westridge Laboratories Inc

Westridge Laboratories Inc — FEI 3003169402

The FDA completed an inspection of Westridge Laboratories Inc on March 20, 2019 in Santa Ana, CA. 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
March 20, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Ana, CA (United States)