# FDA Inspection 1038616 - Biosynergy, Inc. - January 25, 2018

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

> FDA Inspection 1038616 for Biosynergy, Inc. on January 25, 2018. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1038616 - 2018-01-25](https://www.keypedia.com/records/fda_inspections/biosynergy-inc/7b309899-7170-4df3-9634-5f4cf608c822)
- [FDA Inspection 771358 - 2012-03-02](https://www.keypedia.com/records/fda_inspections/biosynergy-inc/83728ab5-f590-4a7c-955b-e7c9a36797e0)
- [FDA Inspection 771358 - 2012-03-02](https://www.keypedia.com/records/fda_inspections/biosynergy-inc/22322e38-7b78-41b8-a968-ef8994fc519c)
- [FDA Inspection 629643 - 2009-11-18](https://www.keypedia.com/records/fda_inspections/biosynergy-inc/18febd71-a6d3-4e41-b603-da6151a46055)

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