# Biosynergy, Inc. – FDA Inspection, Jan 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/biosynergy-inc/ced3dff5-b6fc-407c-bdee-3a6ea528313f
Source feed: FDA_Inspections

> FDA inspection 1038616 of Biosynergy, Inc., January 25, 2018. Classification: Voluntary Action Indicated (VAI). 7 citations 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: 1038616
- Company Name: Biosynergy, Inc.
- Inspection Date: 2018-01-25
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- [FDA Inspection 771358 - 2012-03-02](https://www.keypedia.com/records/fda_inspections/biosynergy-inc/83728ab5-f590-4a7c-955b-e7c9a36797e0)
- [FDA Inspection 629643 - 2009-11-18](https://www.keypedia.com/records/fda_inspections/biosynergy-inc/18febd71-a6d3-4e41-b603-da6151a46055)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/amanda-dinaro/6df79979-ad5c-46f5-8917-197f8a0870e0)
- Issuing Officer

Company: https://www.keypedia.com/companies/biosynergy-inc/4eaf691c-65f4-48bf-bb1e-0f90e12b11fc

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