# FDA Inspection 824388 - Ortho Specialties Inc - March 19, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/ortho-specialties-inc/dce538de-853d-43d9-ad15-a99748c4849c
Source feed: FDA_Inspections

> FDA Inspection 824388 for Ortho Specialties Inc on March 19, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 824388
- Company Name: Ortho Specialties Inc
- Inspection Date: 2013-03-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 824388 - 2013-03-19](https://www.globalkeysolutions.net/records/fda_inspections/ortho-specialties-inc/d9a5832f-38af-492c-9724-4e97916cf9bd)

Company: https://www.globalkeysolutions.net/companies/ortho-specialties-inc/dd8ef56e-8ba7-46a8-b14d-d94f064e1613

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