# FDA Inspection 896205 - Intermed Group, Inc. - September 18, 2014

Source: https://www.keypedia.com/records/fda_inspections/intermed-group-inc/1258a0a7-72e1-4740-b699-d113075ce24c
Source feed: FDA_Inspections

> FDA Inspection 896205 for Intermed Group, Inc. on September 18, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 896205
- Company Name: Intermed Group, Inc.
- Inspection Date: 2014-09-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 754773 - 2011-11-15](https://www.keypedia.com/records/fda_inspections/intermed-group-inc/6c478c5d-c8f2-403b-ac67-27beb8054551)
- [FDA Inspection 754773 - 2011-11-15](https://www.keypedia.com/records/fda_inspections/intermed-group-inc/b8eeff5e-6b5c-4ab6-ada8-23c99362bebc)

Company: https://www.keypedia.com/companies/intermed-group-inc/1d94dec0-ede7-4daa-9072-2320667e947c

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