# OriGen Biomedical, Inc. – FDA Inspection, Jul 5, 2018

Source: https://www.keypedia.com/records/fda_inspections/origen-biomedical-inc/fcae7e18-3d90-4a20-88bf-10fc03ac7b3f
Source feed: FDA_Inspections

> FDA inspection 1059095 of OriGen Biomedical, Inc., July 05, 2018. Classification: Official Action Indicated (OAI). 5 citations under 21 CFR parts 803, 806 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059095
- Company Name: OriGen Biomedical, Inc.
- Inspection Date: 2018-07-05
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- [FDA Inspection 1115852 - 2020-01-08](https://www.keypedia.com/records/fda_inspections/origen-biomedical-inc/58c4e34f-5444-408a-9a2a-b9241ea96457)
- [FDA Inspection 828408 - 2013-04-26](https://www.keypedia.com/records/fda_inspections/origen-biomedical-inc/c701929f-9f68-435e-8797-d3832f2d8d66)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/iris-c-macinnes/5e8d7fef-18d5-453d-82b2-19e8e2897d26)

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