# Sirtex Wilmington LLC – FDA Inspection, Jan 30, 2009

Source: https://www.keypedia.com/records/fda_inspections/sirtex-wilmington-llc/62c043b0-3fba-4705-b16a-f6758b4f14de
Source feed: FDA_Inspections

> FDA inspection 578579 of Sirtex Wilmington LLC, January 30, 2009. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 803. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 578579
- Company Name: Sirtex Wilmington LLC
- Inspection Date: 2009-01-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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Company: https://www.keypedia.com/companies/sirtex-wilmington-llc/6a8f8d3b-3634-4b89-9e79-17447bfbfd29

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