# Fenwal Inc – FDA Inspection, Mar 20, 2009

Source: https://www.keypedia.com/records/fda_inspections/fenwal-inc/8fa0c39e-3e85-4112-832e-b9e9efcc474d
Source feed: FDA_Inspections

> FDA inspection 571368 of Fenwal Inc, March 20, 2009. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 571368
- Company Name: Fenwal Inc
- Inspection Date: 2009-03-20
- 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: 3

## Related Documents

- FDA Inspection 1025637 - 2017-08-07

Company: https://www.keypedia.com/companies/fenwal-inc/d248b9e7-73a7-4054-b268-273a7752c940

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