# Nikomed USA, Inc – FDA Inspection, Dec 1, 2011

Source: https://www.keypedia.com/records/fda_inspections/nikomed-usa-inc/9c5f4998-92f2-47ec-930a-3634891e27f1
Source feed: FDA_Inspections

> FDA inspection 756748 of Nikomed USA, Inc, December 01, 2011. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 756748
- Company Name: Nikomed USA, Inc
- Inspection Date: 2011-12-01
- 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 1000189 - 2017-02-06](https://www.keypedia.com/records/fda_inspections/nikomed-usa-inc/ca632cf4-af07-422f-a772-03c2b1e4d3bc)
- [FDA Inspection 546209 - 2008-10-09](https://www.keypedia.com/records/fda_inspections/nikomed-usa-inc/efa74c6a-ee45-44c9-8751-5886d8448d1a)

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
