FDA Inspection
Intronix Technologies CorporationIntronix Technologies Corporation – FDA Inspection, Feb 26, 2015
Record Details
This FDA Inspection record concerns Intronix Technologies Corporation, with an inspection on February 26, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- February 26, 2015
- Product Type
- Devices
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ID · 61f9b797-fdb6-4639-9a42-b7ba4e412462
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 920702
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
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Other FDA inspections of Intronix Technologies Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| February 7, 2018 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
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