FDA Inspection 1323306 — Entrogen, Inc

Entrogen, Inc — FEI 3010791816

The FDA completed an inspection of Entrogen, Inc on May 14, 2026 in Woodland Hills, 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
May 14, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Woodland Hills, CA (United States)