# FDA Inspection 813877 - The Flexite Company - January 09, 2013

Source: https://www.keypedia.com/records/fda_inspections/the-flexite-company/97f86187-2fa1-4e96-a982-cfa2c801a5b7
Source feed: FDA_Inspections

> FDA Inspection 813877 for The Flexite Company on January 09, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 813877
- Company Name: The Flexite Company
- Inspection Date: 2013-01-09
- 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.keypedia.com/companies/the-flexite-company/c095b520-5859-4ec0-98fd-901e5f733bb5

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