FDA Inspection 1216536 — Entrogen, Inc

Entrogen, Inc — FEI 3010791816

The FDA completed an inspection of Entrogen, Inc on July 31, 2023 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
July 31, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Woodland Hills, CA (United States)