FDA Inspection 1297462 — Imvaria Inc.

Imvaria Inc. — FEI 3033729853

The FDA completed an inspection of Imvaria Inc. on Dec 3, 2025 in Berkeley, 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
Dec 3, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Berkeley, CA (United States)

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