# Gendron Inc. – FDA Inspection, Sep 11, 2009

Source: https://www.keypedia.com/records/fda_inspections/gendron-inc/d9ce86b3-43cf-4c85-adb3-b7c05b4bd2a1
Source feed: FDA_Inspections

> FDA inspection 612343 of Gendron Inc., September 11, 2009. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 612343
- Company Name: Gendron Inc.
- Inspection Date: 2009-09-11
- 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: 3

## Related Documents

- [FDA Inspection 1044724 - 2018-03-16](https://www.keypedia.com/records/fda_inspections/gendron-inc/f3e6ca01-1bd8-43f2-8a2b-62e9c9d97663)
- FDA Inspection 885340 - 2014-07-02

Company: https://www.keypedia.com/companies/gendron-inc/c6dbe980-a47f-4959-ac00-9e78ec140102

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