FDA Inspection
Dujo Logos IncDujo Logos Inc – FDA Inspection, Jan 4, 2018
Record Details
This FDA Inspection record concerns Dujo Logos Inc, with an inspection on January 4, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · f2234739-760d-4e50-9c16-ff1d76a4e739
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1038139
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Dujo Logos Inc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 16, 2026 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 2, 2022 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 24, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 6, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 22, 2010 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Dujo Logos Inc
- FDA Inspection 1338266 - 2026-09-16
- FDA Inspection 1172530 - 2022-06-02
- FDA Inspection 937609 - 2015-06-24
- FDA Inspection 766353 - 2012-02-06
- FDA Inspection 647582 - 2010-02-22
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