# Gold Standard Diagnostics – FDA Inspection, Sep 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/gold-standard-diagnostics/6dffab00-930e-4a5b-a2e0-3c0890323710
Source feed: FDA_Inspections

> FDA inspection 1025850 of Gold Standard Diagnostics, September 13, 2017. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1025850
- Company Name: Gold Standard Diagnostics
- Inspection Date: 2017-09-13
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1096364 - 2018-12-05](https://www.keypedia.com/records/fda_inspections/gold-standard-diagnostics/b59e57ce-8ff3-4f5d-9053-021a9010daa6)
- FDA Inspection 903290 - 2014-11-07
- [FDA Inspection 859740 - 2013-12-20](https://www.keypedia.com/records/fda_inspections/gold-standard-diagnostics/82da1995-d625-4bd2-8cc0-d71eb39a262e)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/mark-e-chan/2a5a3abf-96f6-4ceb-b87d-379ed5c6f47e)

Company: https://www.keypedia.com/companies/gold-standard-diagnostics/35a18b61-b8ce-433f-8958-f55c361c2962

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