FDA Inspection 1320562 — Prowess, Inc.

Prowess, Inc. — FEI 2939248

The FDA completed an inspection of Prowess, Inc. on June 2, 2026 in Concord, 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
June 2, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Concord, CA (United States)