# Philips Ultrasound, Inc. – FDA Inspection, Dec 9, 2011

Source: https://www.keypedia.com/records/fda_inspections/philips-ultrasound-inc/51fecd2b-2e1f-4c13-89af-c20ab779a51c
Source feed: FDA_Inspections

> FDA inspection 761739 of Philips Ultrasound, Inc., December 09, 2011. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 761739
- Company Name: Philips Ultrasound, Inc.
- Inspection Date: 2011-12-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

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Company: https://www.keypedia.com/companies/philips-ultrasound-inc/36d048c6-d991-443c-b562-f9d7bacc8be8

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