# FDA Inspection 938132 - Zevex, Inc. - July 30, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/zevex-inc/626f4cdc-714f-4666-a4c3-1731e58b702e
Source feed: FDA_Inspections

> FDA Inspection 938132 for Zevex, Inc. on July 30, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 938132
- Company Name: Zevex, Inc.
- Inspection Date: 2015-07-30
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 938132 - 2015-07-30](https://www.globalkeysolutions.net/records/fda_inspections/zevex-inc/cf76a41c-57d6-4017-a8bb-bb1717cd5f73)

Company: https://www.globalkeysolutions.net/companies/zevex-inc/59d978f3-677b-4233-b46a-801d6e70bb56

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