# Douglas Medical Products, Inc. – FDA Inspection, Sep 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 of Douglas Medical Products, Inc., September 21, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1323366 - 2026-06-24](https://www.keypedia.com/records/fda_inspections/douglas-medical-products-inc/32b735d3-cbeb-4c5b-99dd-b046624c8d9a)
- FDA Inspection 1160698 - 2021-12-14

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

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