# The Flexite Company – FDA Inspection, Nov 19, 2015

Source: https://www.keypedia.com/records/fda_inspections/the-flexite-company/4ed0a874-d47d-4c31-8e96-12e72c73bbed
Source feed: FDA_Inspections

> FDA inspection 951140 of The Flexite Company, November 19, 2015. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 951140
- Company Name: The Flexite Company
- Inspection Date: 2015-11-19
- 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: 4

## Related Documents

- FDA Inspection 1172026 - 2022-06-01
- [FDA Inspection 1068392 - 2018-10-05](https://www.keypedia.com/records/fda_inspections/the-flexite-company/b125821a-2411-437e-9560-233e332b70b7)
- [FDA Inspection 813877 - 2013-01-09](https://www.keypedia.com/records/fda_inspections/the-flexite-company/97f86187-2fa1-4e96-a982-cfa2c801a5b7)
- [FDA Inspection 706613 - 2011-01-19](https://www.keypedia.com/records/fda_inspections/the-flexite-company/6c9fb47f-a0cd-4605-a9d3-d6586cc990a9)
- FDA Inspection 541724 - 2008-10-08

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