# NAMSA – FDA Inspection, May 18, 2018

Source: https://www.keypedia.com/records/fda_inspections/namsa/abf563d6-f014-4fbf-9ec9-0964b6e04e07
Source feed: FDA_Inspections

> FDA inspection 1052433 of NAMSA, May 18, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1052433
- Company Name: NAMSA
- Inspection Date: 2018-05-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1197992 - 2023-02-08
- FDA Inspection 1002871 - 2017-02-16
- [FDA Inspection 819156 - 2013-02-04](https://www.keypedia.com/records/fda_inspections/namsa/6fc21266-c02e-4542-821a-7d8028eca13b)
- [FDA Inspection 676437 - 2010-09-03](https://www.keypedia.com/records/fda_inspections/namsa/edbe69df-7b84-44ef-b60e-8a2feb519632)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/nicole-c-victoria/8c5f8060-452f-4fe5-a43f-a448ec020e60)

Company: https://www.keypedia.com/companies/namsa/f682195b-ca54-4a02-b106-71b74e647b2e

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