# FDA Inspection 855722 - The GID Group, Inc. - November 12, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/the-gid-group-inc/f91df5e6-57e8-4a58-a31b-75bc826ae0bc
Source feed: FDA_Inspections

> FDA Inspection 855722 for The GID Group, Inc. on November 12, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 855722
- Company Name: The GID Group, Inc.
- Inspection Date: 2013-11-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 992733 - 2016-11-29](https://www.globalkeysolutions.net/records/fda_inspections/the-gid-group-inc/5630379d-54e7-47e1-8cd4-f208c8134b84)
- [FDA Inspection 855722 - 2013-11-12](https://www.globalkeysolutions.net/records/fda_inspections/the-gid-group-inc/07c18136-cdd2-4013-836e-5b7629a67df4)

Company: https://www.globalkeysolutions.net/companies/the-gid-group-inc/01020ace-08b4-4b7c-89e6-2918fe650908

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