# Orthoscan, Inc. – FDA Inspection, Mar 26, 2009

Source: https://www.keypedia.com/records/fda_inspections/orthoscan-inc/acea5f3a-ee23-4dbc-a75a-436c4a1581a8
Source feed: FDA_Inspections

> FDA inspection 572311 of Orthoscan, Inc., March 26, 2009. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 572311
- Company Name: Orthoscan, Inc.
- Inspection Date: 2009-03-26
- 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 1076842 - 2018-11-20
- FDA Inspection 1106197 - 2018-11-01
- FDA Inspection 913100 - 2015-01-23
- FDA Inspection 783031 - 2012-05-24

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

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