# Intermed Group, Inc. – FDA Inspection, Sep 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 of Intermed Group, Inc., September 18, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 754773 - 2011-11-15

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