# FDA Inspection 884755 - Westmed, Inc. - June 18, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/westmed-inc/d9b6d0b0-ca6c-451f-81e8-27306fbfb961
Source feed: FDA_Inspections

> FDA Inspection 884755 for Westmed, Inc. on June 18, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 884755
- Company Name: Westmed, Inc.
- Inspection Date: 2014-06-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1113006 - 2019-12-11](https://www.globalkeysolutions.net/records/fda_inspections/westmed-inc/05b67fcb-f9e3-45a6-99dc-51f388322bf2)
- [FDA Inspection 1113006 - 2019-12-11](https://www.globalkeysolutions.net/records/fda_inspections/westmed-inc/0c34576b-d095-42f5-941f-23f1e369dc11)
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Company: https://www.globalkeysolutions.net/companies/westmed-inc/0d999e50-c2aa-49cf-ac37-123c84f600ea

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