# FDA Inspection 933138 - NYOrtho - July 01, 2015

Source: https://www.keypedia.com/records/fda_inspections/nyortho/1cf912eb-d460-456c-ba4a-2cb6d2cdbdfe
Source feed: FDA_Inspections

> FDA Inspection 933138 for NYOrtho on July 01, 2015. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 933138 - 2015-07-01](https://www.keypedia.com/records/fda_inspections/nyortho/748fcf4f-5292-4bc4-9499-0fb205a40d3a)

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