FDA Inspection
Douglas Medical Products, Inc.Douglas Medical Products, Inc. – FDA Inspection, Sep 21, 2017
Record Details
This FDA Inspection record concerns Douglas Medical Products, Inc., with an inspection on September 21, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 7bcc248d-dfe7-4e05-86af-d908c8759d3c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1026575
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.198(a)Complaints
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Douglas Medical Products, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 24, 2026 | Not classified | Chicago District Office | Compliance: Devices |
| December 14, 2021 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Douglas Medical Products, Inc.
- FDA Inspection 1323366 - 2026-06-24
- FDA Inspection 1160698 - 2021-12-14
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