FDA Inspection 1167584 — Agendia, Inc.

Agendia, Inc. — FEI 3007297853

The FDA completed an inspection of Agendia, Inc. on April 12, 2022 in Irvine, 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
April 12, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)