# NYOrtho – FDA Inspection, Jul 1, 2015

Source: https://www.keypedia.com/records/fda_inspections/nyortho/748fcf4f-5292-4bc4-9499-0fb205a40d3a
Source feed: FDA_Inspections

> FDA inspection 933138 of NYOrtho, July 01, 2015. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 933138
- Company Name: NYOrtho
- Inspection Date: 2015-07-01
- 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

Company: https://www.keypedia.com/companies/nyortho/cd62bb65-1f04-4b6d-bda8-34d85fa9e3ff

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