# FDA Inspection 1026575 - Douglas Medical Products, Inc. - September 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/douglas-medical-products-inc/7bcc248d-dfe7-4e05-86af-d908c8759d3c
Source feed: FDA_Inspections

> FDA Inspection 1026575 for Douglas Medical Products, Inc. on September 21, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026575
- Company Name: Douglas Medical Products, Inc.
- Inspection Date: 2017-09-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1160698 - 2021-12-14](https://www.keypedia.com/records/fda_inspections/douglas-medical-products-inc/88c39f7b-42c6-4cdb-9da5-111bf5a0596f)
- [FDA Inspection 1160698 - 2021-12-14](https://www.keypedia.com/records/fda_inspections/douglas-medical-products-inc/e5915620-60cb-40e0-802f-827ca3fcd444)

Company: https://www.keypedia.com/companies/douglas-medical-products-inc/bb54cbf9-d480-4877-a305-6fc6febc01dc

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