# Avantis Medical – FDA Inspection, Jul 24, 2009

Source: https://www.keypedia.com/records/fda_inspections/avantis-medical/517ae3a9-3ef4-4bd4-9a87-7b2f5fed435b
Source feed: FDA_Inspections

> FDA inspection 620295 of Avantis Medical, July 24, 2009. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 620295
- Company Name: Avantis Medical
- Inspection Date: 2009-07-24
- 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: 6

## Related Documents

- FDA Inspection 983344 - 2016-03-10
- FDA Inspection 785019 - 2012-06-08

Company: https://www.keypedia.com/companies/avantis-medical/535ad3e5-2cdd-47e6-aca1-def83ab3050e

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