# NuTech Spine, Inc. – FDA Inspection, Jun 20, 2019

Source: https://www.keypedia.com/records/fda_inspections/nutech-spine-inc/95477789-df9a-42ca-9226-3a7b1e415c8a
Source feed: FDA_Inspections

> FDA inspection 1094097 of NuTech Spine, Inc., June 20, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1094097
- Company Name: NuTech Spine, Inc.
- Inspection Date: 2019-06-20
- 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: 1

## Related Documents

- FDA Inspection 1155920 - 2021-10-27
- FDA Inspection 1056306 - 2018-04-25
- FDA Inspection 982009 - 2016-07-13
- FDA Inspection 884316 - 2014-06-18
- FDA Inspection 833696 - 2013-04-30

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/nutech-spine-inc/7864b0cd-7cf7-490b-b55a-82d524ac8c7e

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