# FDA Inspection 571368 - Fenwal Inc - March 20, 2009

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

> FDA Inspection 571368 for Fenwal Inc on March 20, 2009. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1025637 - 2017-08-07](https://www.keypedia.com/records/fda_inspections/fenwal-inc/53ed7871-8be9-4cc1-a533-81adcca4e5c7)
- [FDA Inspection 1025637 - 2017-08-07](https://www.keypedia.com/records/fda_inspections/fenwal-inc/fa93e337-a3dd-4946-88eb-f27a9056dc3e)

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