# FDA Inspection 572311 - Orthoscan, Inc. - March 26, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/orthoscan-inc/3af8e641-d6e2-4ca9-aa0e-36b0fee92c7e
Source feed: FDA_Inspections

> FDA Inspection 572311 for Orthoscan, Inc. on March 26, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 572311
- Company Name: Orthoscan, Inc.
- Inspection Date: 2009-03-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 572311 - 2009-03-26](https://www.globalkeysolutions.net/records/fda_inspections/orthoscan-inc/acea5f3a-ee23-4dbc-a75a-436c4a1581a8)

Company: https://www.globalkeysolutions.net/companies/orthoscan-inc/a4ca0d4b-8eaa-49fc-b496-cd35ea801557

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