# FDA Inspection 592352 - Diacor, Inc - June 25, 2009

Source: https://www.keypedia.com/records/fda_inspections/diacor-inc/0ae044d4-0d9f-45df-9138-cd3fa32c4e48
Source feed: FDA_Inspections

> FDA Inspection 592352 for Diacor, Inc on June 25, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 592352
- Company Name: Diacor, Inc
- Inspection Date: 2009-06-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/diacor-inc/11688ab9-29f4-4edd-9d07-82c11bec238a

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