# NextPhase Medical Devices – FDA Inspection, Dec 6, 2016

Source: https://www.keypedia.com/records/fda_inspections/nextphase-medical-devices/b88c1ebd-6e1e-4bf7-abe9-6db8ce540a1e
Source feed: FDA_Inspections

> FDA inspection 998478 of NextPhase Medical Devices, December 06, 2016. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998478
- Company Name: NextPhase Medical Devices
- Inspection Date: 2016-12-06
- 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: 2

## Related Documents

- [FDA Inspection 787295 - 2012-06-21](https://www.keypedia.com/records/fda_inspections/nextphase-medical-devices/f54d8fa8-64ad-4a93-b8a9-5177f11c3367)
- FDA Inspection 608671 - 2009-08-18
- FDA Inspection 550580 - 2008-12-05

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/david-h-smith/a78c3b20-1fb4-438f-904b-a6ab51a81945)

Company: https://www.keypedia.com/companies/nextphase-medical-devices/b0a447a9-c125-4752-857e-7314547ecb43

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