# Orthosensor, Inc. – FDA Inspection, May 24, 2012

Source: https://www.keypedia.com/records/fda_inspections/orthosensor-inc/56688fd7-f185-479e-a3b8-3f9992dc1aba
Source feed: FDA_Inspections

> FDA inspection 784081 of Orthosensor, Inc., May 24, 2012. Classification: No Action Indicated (NAI). 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 784081
- Company Name: Orthosensor, Inc.
- Inspection Date: 2012-05-24
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 956163 - 2016-01-15

Company: https://www.keypedia.com/companies/orthosensor-inc/c3b0a6a8-09d1-4c15-86c7-af9cb2fd88fe

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