# Sonogage Inc – FDA Inspection, Jul 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/sonogage-inc/c8bb3d0b-eacf-4350-9cc5-9baa13131b95
Source feed: FDA_Inspections

> FDA inspection 843975 of Sonogage Inc, July 26, 2013. Classification: Voluntary Action Indicated (VAI). 11 citations under 21 CFR parts 108 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 843975
- Company Name: Sonogage Inc
- Inspection Date: 2013-07-26
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 11

## Related Documents

- FDA Inspection 1203721 - 2023-04-25
- [FDA Inspection 1045173 - 2018-03-21](https://www.keypedia.com/records/fda_inspections/sonogage-inc/a345fc01-54bb-4924-9195-22be473640bb)
- FDA Inspection 895282 - 2014-09-12
- FDA Inspection 601020 - 2009-07-31

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