# FDA Inspection 973519 - Gf Health Products - March 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/gf-health-products/5da35240-bf62-4131-8e4d-c87ac942c108
Source feed: FDA_Inspections

> FDA Inspection 973519 for Gf Health Products on March 25, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 973519
- Company Name: Gf Health Products
- Inspection Date: 2016-03-25
- 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 973519 - 2016-03-25](https://www.keypedia.com/records/fda_inspections/gf-health-products/8de9fca4-36af-4740-ba92-73cdf43de00e)
- [FDA Inspection 771670 - 2012-03-07](https://www.keypedia.com/records/fda_inspections/gf-health-products/c382e434-0295-4181-979d-673b1872407e)
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- [FDA Inspection 668423 - 2010-06-03](https://www.keypedia.com/records/fda_inspections/gf-health-products/23e469a9-c9dc-4223-8aa5-fa57a706d06e)

Company: https://www.keypedia.com/companies/gf-health-products/87931bd8-6675-4ee0-85c5-860d98f6edd1

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