# FDA Inspection 612343 - Gendron Inc. - September 11, 2009

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

> FDA Inspection 612343 for Gendron Inc. on September 11, 2009. Classification: Voluntary Action Indicated (VAI).

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

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

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