# FDA Inspection 1025637 - Fenwal Inc - August 07, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/fenwal-inc/fa93e337-a3dd-4946-88eb-f27a9056dc3e/
Source feed: FDA_Inspections

> FDA Inspection 1025637 for Fenwal Inc on August 07, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025637
- Company Name: Fenwal Inc
- Inspection Date: 2017-08-07
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1025637 - 2017-08-07](https://www.globalkeysolutions.net/api/records/fda_inspections/fenwal-inc/53ed7871-8be9-4cc1-a533-81adcca4e5c7/)
- [FDA Inspection 571368 - 2009-03-20](https://www.globalkeysolutions.net/api/records/fda_inspections/fenwal-inc/8fa0c39e-3e85-4112-832e-b9e9efcc474d/)

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

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