FDA Inspection 1115852 — OriGen Biomedical, Inc.

OriGen Biomedical, Inc. — FEI 1000160256

The FDA completed an inspection of OriGen Biomedical, Inc. on January 8, 2020 in Austin, TX. 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
January 8, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Austin, TX (United States)