# Genesee BioMedical, Inc. – FDA Inspection, Feb 9, 2018

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

> FDA inspection 1040396 of Genesee BioMedical, Inc., February 09, 2018. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 806 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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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)
- 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: 3

## Related Documents

- FDA Inspection 707252 - 2011-01-25

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/vicky-l-cruz/282da571-56be-48f4-96c6-d590829b12c2)

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