# Goldway (US), Inc – FDA Inspection, Sep 11, 2009

Source: https://www.keypedia.com/records/fda_inspections/goldway-us-inc/6f0b497b-7dd8-443e-833e-4323eb22ab2a
Source feed: FDA_Inspections

> FDA inspection 612178 of Goldway (US), Inc, September 11, 2009. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 612178
- Company Name: Goldway (US), Inc
- Inspection Date: 2009-09-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 898886 - 2014-10-02
- FDA Inspection 778942 - 2012-04-26

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