FDA Inspection 1239086 — PHENOX INC

PHENOX INC — FEI 3015543504

The FDA completed an inspection of PHENOX INC on Apr 11, 2024 in Irvine, 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
Apr 11, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Irvine, CA (United States)

Additional Details

Sponsor, Contract Research Organization