# FDA Inspection 784081 - Orthosensor, Inc. - May 24, 2012

Source: https://www.keypedia.com/records/fda_inspections/orthosensor-inc/403c7ca6-eb8f-40ac-9c0a-a7381074eaa7
Source feed: FDA_Inspections

> FDA Inspection 784081 for Orthosensor, Inc. on May 24, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 784081
- Company Name: Orthosensor, Inc.
- Inspection Date: 2012-05-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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