# FDA Inspection 898886 - Goldway (US), Inc - October 02, 2014

Source: https://www.keypedia.com/records/fda_inspections/goldway-us-inc/58de4305-255e-40f1-86f8-ffc5ea415ff2
Source feed: FDA_Inspections

> FDA Inspection 898886 for Goldway (US), Inc on October 02, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 898886
- Company Name: Goldway (US), Inc
- Inspection Date: 2014-10-02
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/goldway-us-inc/6530df0e-16bb-4e53-9539-264547145509

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