# FDA Inspection 821656 - Exel, Inc. - February 21, 2013

Source: https://www.keypedia.com/records/fda_inspections/exel-inc/fb2eb334-68f9-4f96-b9e3-b6672c3aaa7d
Source feed: FDA_Inspections

> FDA Inspection 821656 for Exel, Inc. on February 21, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 821656
- Company Name: Exel, Inc.
- Inspection Date: 2013-02-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 640742 - 2010-01-06](https://www.keypedia.com/records/fda_inspections/exel-inc/08f91072-62eb-4f17-8a09-dc5a308f37af)

Company: https://www.keypedia.com/companies/exel-inc/5f91bff9-219a-49f4-9613-d6ca833dad9a

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