FDA Inspection
Linxens Sweden ABLinxens Sweden AB – FDA Inspection, Nov 7, 2024
Record Details
This FDA Inspection record concerns Linxens Sweden AB, with an inspection on November 7, 2024, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c70c3636-006d-45f2-8431-ea6a5427bcf8
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1253832
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.75(a)Documentation
- 21 CFR 820.30(h)Design transfer - Lack of or inadequate procedures
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