FDA Inspection 1246794 — Accriva Diagnostics, Inc.

Accriva Diagnostics, Inc. — FEI 2250033

The FDA completed an inspection of Accriva Diagnostics, Inc. on July 19, 2024 in San Diego, 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
July 19, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Diego, CA (United States)