# Nikomed USA, Inc – FDA Inspection, Feb 6, 2017

Source: https://www.keypedia.com/records/fda_inspections/nikomed-usa-inc/ca632cf4-af07-422f-a772-03c2b1e4d3bc
Source feed: FDA_Inspections

> FDA inspection 1000189 of Nikomed USA, Inc, February 06, 2017. Classification: Voluntary Action Indicated (VAI). 3 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: 1000189
- Company Name: Nikomed USA, Inc
- Inspection Date: 2017-02-06
- 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: 3

## Related Documents

- [FDA Inspection 756748 - 2011-12-01](https://www.keypedia.com/records/fda_inspections/nikomed-usa-inc/9c5f4998-92f2-47ec-930a-3634891e27f1)
- [FDA Inspection 546209 - 2008-10-09](https://www.keypedia.com/records/fda_inspections/nikomed-usa-inc/efa74c6a-ee45-44c9-8751-5886d8448d1a)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/raffi-b-papazian/c2a5ca35-87d9-46cf-99eb-12fd455b7e68)

Company: https://www.keypedia.com/companies/nikomed-usa-inc/d0158e49-2a46-463e-ba47-5e6522fbb25a

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