# InteloMed, Inc. – FDA Inspection, Feb 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/intelomed-inc/544311b4-d4fb-4d21-a4b5-1dcbbebe1358
Source feed: FDA_Inspections

> FDA inspection 1012237 of InteloMed, Inc., February 28, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1012237
- Company Name: InteloMed, Inc.
- Inspection Date: 2017-02-28
- 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: 0

## Related Documents

- FDA Inspection 1117890 - 2020-01-15

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/katelyn-a-staub-zamperini/bb7f95a4-53c1-473c-856e-517312bdba30)

Company: https://www.keypedia.com/companies/intelomed-inc/f6db03ca-d4f1-4451-b705-e9de0458dafd

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