# FDA Inspection 1085079 - Flexicare, Inc. - April 04, 2019

Source: https://www.keypedia.com/records/fda_inspections/flexicare-inc/c16e57c7-dc22-4b15-a39a-7ed77280fe2e
Source feed: FDA_Inspections

> FDA Inspection 1085079 for Flexicare, Inc. on April 04, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1085079
- Company Name: Flexicare, Inc.
- Inspection Date: 2019-04-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1085079 - 2019-04-04](https://www.keypedia.com/records/fda_inspections/flexicare-inc/0b2bc3fd-5b93-4fbe-b540-c26691a8672e)

Company: https://www.keypedia.com/companies/flexicare-inc/7bf19e08-1120-47b9-a761-7741f9af5ccc

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