# FDA Inspection 1100180 - Whitney Products Inc. - August 22, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/whitney-products-inc/334da201-acde-43fe-afd8-0ccc17f53d4d
Source feed: FDA_Inspections

> FDA Inspection 1100180 for Whitney Products Inc. on August 22, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100180
- Company Name: Whitney Products Inc.
- Inspection Date: 2019-08-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100180 - 2019-08-22](https://www.globalkeysolutions.net/records/fda_inspections/whitney-products-inc/d28e697a-1303-433a-84e7-45ca14642ee0)
- [FDA Inspection 915978 - 2015-02-18](https://www.globalkeysolutions.net/records/fda_inspections/whitney-products-inc/4ab790f0-222d-4671-a4d7-571ae42c66d3)
- [FDA Inspection 915978 - 2015-02-18](https://www.globalkeysolutions.net/records/fda_inspections/whitney-products-inc/8fb4c221-aa93-4e93-96af-76a953797067)

Company: https://www.globalkeysolutions.net/companies/whitney-products-inc/442af0c2-292d-4ef4-8f53-0f79feefd56f

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