# Immco Diagnostics, Inc. – FDA Inspection, Jul 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/immco-diagnostics-inc/141a7514-3e67-4185-b089-30537de715f4
Source feed: FDA_Inspections

> FDA inspection 1018931 of Immco Diagnostics, Inc., July 20, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018931
- Company Name: Immco Diagnostics, Inc.
- Inspection Date: 2017-07-20
- 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 822060 - 2013-03-13
- FDA Inspection 717119 - 2011-03-22

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/matthew-d-schnittker/cf76f07f-db6d-47a0-8412-7eb084d4fe8b)

Company: https://www.keypedia.com/companies/immco-diagnostics-inc/30985789-b7fc-45a2-8cab-a481674b50c0

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