# FDA Inspection 1000189 - Nikomed USA, Inc - February 06, 2017

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

> FDA Inspection 1000189 for Nikomed USA, Inc on February 06, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## 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 756748 - 2011-12-01](https://www.keypedia.com/records/fda_inspections/nikomed-usa-inc/67175b3c-a0c4-4f14-b995-22ca5d6925fb)
- [FDA Inspection 546209 - 2008-10-09](https://www.keypedia.com/records/fda_inspections/nikomed-usa-inc/efa74c6a-ee45-44c9-8751-5886d8448d1a)
- [FDA Inspection 546209 - 2008-10-09](https://www.keypedia.com/records/fda_inspections/nikomed-usa-inc/54be5051-5f0c-4b9c-a0b4-22834e915c6f)

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