# FDA Inspection 1015191 - FlexDex Inc. - June 22, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/flexdex-inc/ff515bac-4e9f-40c0-aec8-80e05a76ac5a/
Source feed: FDA_Inspections

> FDA Inspection 1015191 for FlexDex Inc. on June 22, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015191
- Company Name: FlexDex Inc.
- Inspection Date: 2017-06-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1015191 - 2017-06-22](https://www.globalkeysolutions.net/api/records/fda_inspections/flexdex-inc/4022778d-fd18-422a-8dec-45cab1fc0e16/)

Company: https://www.globalkeysolutions.net/companies/flexdex-inc/a2369927-5ba8-4328-9a0f-d52f3e6d83a6

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