FDA Inspection
Silq Technologies CorporationSilq Technologies Corporation – FDA Inspection, Jan 5, 2023
Record Details
This FDA Inspection record concerns Silq Technologies Corporation, with an inspection on January 5, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · b05be1b7-abe5-4029-8ffb-e0abdf3bd87e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1194223
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.20(c)Management review - defined interval, sufficient frequency
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Other FDA inspections of Silq Technologies Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| October 16, 2025 | VAI | Florida District Office | Compliance: Medical Devices |
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