# FDA Inspection 578166 - Flex Technology, Inc. - April 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/flex-technology-inc/cffbeac0-fef5-468a-82ce-d451194c9980
Source feed: FDA_Inspections

> FDA Inspection 578166 for Flex Technology, Inc. on April 09, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 578166
- Company Name: Flex Technology, Inc.
- Inspection Date: 2009-04-09
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/flex-technology-inc/e7f34d1f-a72d-44d6-9cb0-7ceb26d45720

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