# FDA Inspection 1040396 - Genesee BioMedical, Inc. - February 09, 2018

Source: https://www.keypedia.com/records/fda_inspections/genesee-biomedical-inc/bf06b93f-d2f9-40ee-b409-d764d34a4be9
Source feed: FDA_Inspections

> FDA Inspection 1040396 for Genesee BioMedical, Inc. on February 09, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040396
- Company Name: Genesee BioMedical, Inc.
- Inspection Date: 2018-02-09
- 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 1040396 - 2018-02-09](https://www.keypedia.com/records/fda_inspections/genesee-biomedical-inc/89acc55d-ad22-4019-a36c-1375a2cd1f4d)
- [FDA Inspection 707252 - 2011-01-25](https://www.keypedia.com/records/fda_inspections/genesee-biomedical-inc/8f496891-ef37-457f-b266-63212dc068b1)
- [FDA Inspection 707252 - 2011-01-25](https://www.keypedia.com/records/fda_inspections/genesee-biomedical-inc/90ead842-05b0-4d58-97ae-54093e2884d6)

Company: https://www.keypedia.com/companies/genesee-biomedical-inc/c321d66d-1b00-4e30-9cdf-ddee6a6ec502

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