# FDA Inspection 1059384 - Eastwestmed, Inc. - July 03, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/eastwestmed-inc/29a01491-664a-49c7-881a-30f2960c5efd
Source feed: FDA_Inspections

> FDA Inspection 1059384 for Eastwestmed, Inc. on July 03, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1059384
- Company Name: Eastwestmed, Inc.
- Inspection Date: 2018-07-03
- 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 1059384 - 2018-07-03](https://www.globalkeysolutions.net/records/fda_inspections/eastwestmed-inc/bc7d663d-7379-47b7-8181-397ea9871ada)
- [FDA Inspection 738479 - 2011-08-10](https://www.globalkeysolutions.net/records/fda_inspections/eastwestmed-inc/a3635d56-b86b-44c3-bfef-255d1ea9a108)
- [FDA Inspection 738479 - 2011-08-10](https://www.globalkeysolutions.net/records/fda_inspections/eastwestmed-inc/1800910c-9fb3-4a11-8f87-c711a862f906)

Company: https://www.globalkeysolutions.net/companies/eastwestmed-inc/1c82aefb-c259-45a7-85ab-b1a3b3eedc58

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