FDA Inspection 1074241 — Biophotas, Inc

Biophotas, Inc — FEI 3009765778

The FDA completed an inspection of Biophotas, Inc on November 27, 2018 in Tustin, 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
November 27, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tustin, CA (United States)

Additional Details

Sponsor, Contract Research Organization