# OriGen Biomedical, Inc. – FDA Inspection, Jan 8, 2020

Source: https://www.keypedia.com/records/fda_inspections/origen-biomedical-inc/58c4e34f-5444-408a-9a2a-b9241ea96457
Source feed: FDA_Inspections

> FDA inspection 1115852 of OriGen Biomedical, Inc., January 08, 2020. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1115852
- Company Name: OriGen Biomedical, Inc.
- Inspection Date: 2020-01-08
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1059095 - 2018-07-05](https://www.keypedia.com/records/fda_inspections/origen-biomedical-inc/fcae7e18-3d90-4a20-88bf-10fc03ac7b3f)
- [FDA Inspection 828408 - 2013-04-26](https://www.keypedia.com/records/fda_inspections/origen-biomedical-inc/c701929f-9f68-435e-8797-d3832f2d8d66)

Company: https://www.keypedia.com/companies/origen-biomedical-inc/6d4f9178-e02c-4ba8-9820-40f0fb5d7080

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7