# FDA Inspection 807456 - Parkway Products, Inc. - November 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/parkway-products-inc/b4c7fe50-a353-4b6e-848a-05821a5268d6
Source feed: FDA_Inspections

> FDA Inspection 807456 for Parkway Products, Inc. on November 20, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 807456
- Company Name: Parkway Products, Inc.
- Inspection Date: 2012-11-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 807456 - 2012-11-20](https://www.keypedia.com/records/fda_inspections/parkway-products-inc/053a379d-4cf1-4282-9c61-5f2ad0c424ef)
- [FDA Inspection 547721 - 2008-11-13](https://www.keypedia.com/records/fda_inspections/parkway-products-inc/9ea8fbba-7b31-4621-8de2-631401af5917)

Company: https://www.keypedia.com/companies/parkway-products-inc/c85d19da-5712-4ee0-8190-413701dbb852

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