# FDA Inspection 601020 - Sonogage Inc - July 31, 2009

Source: https://www.keypedia.com/records/fda_inspections/sonogage-inc/4dfb29cc-e691-4831-9ee7-c4c7ea12d9a1
Source feed: FDA_Inspections

> FDA Inspection 601020 for Sonogage Inc on July 31, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 601020
- Company Name: Sonogage Inc
- Inspection Date: 2009-07-31
- 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/sonogage-inc/507a083b-aae2-4afd-bd78-611513df43c5

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