FDA Inspection
PATHWAY MEDTECH, LLCPATHWAY MEDTECH, LLC – FDA Inspection, May 22, 2024
Record Details
This FDA Inspection record concerns PATHWAY MEDTECH, LLC, with an inspection on May 22, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · fa2c1e3d-2e6b-47e8-a755-1b7c8bc7edb0
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1239270
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- Devices subject to device identification GUDID data submission requirements.
- 21 CFR 830.300(a)Devices subject to device identification GUDID data submission requirements.
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Other FDA inspections of PATHWAY MEDTECH, LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| August 3, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for PATHWAY MEDTECH, LLC
- FDA Inspection 1062131 - 2018-08-03
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