FDA Inspection 1246794 — Accriva Diagnostics, Inc.

Accriva Diagnostics, Inc. — FEI 2250033

The FDA completed an inspection of Accriva Diagnostics, Inc. on Jul 19, 2024 in San Diego, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 19, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
San Diego, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.