# Bio Gen Technologies, Inc – FDA Inspection, Apr 10, 2018

Source: https://www.keypedia.com/records/fda_inspections/bio-gen-technologies-inc/f5231732-44d6-467c-8ac4-7fb6f982bf48
Source feed: FDA_Inspections

> FDA inspection 1048028 of Bio Gen Technologies, Inc, April 10, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1048028
- Company Name: Bio Gen Technologies, Inc
- Inspection Date: 2018-04-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1247229 - 2024-08-16](https://www.keypedia.com/records/fda_inspections/bio-gen-technologies-inc/0014f035-37d1-4234-a9ab-7b576c6d27bf)
- FDA Inspection 1152302 - 2021-09-16

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/nicholas-c-mendiola/387f053a-af5f-4da9-8042-031124b9467d)

Company: https://www.keypedia.com/companies/bio-gen-technologies-inc/1d0bbcde-0cdc-4fba-8371-7bc6252f5d1a

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