FDA Inspection
InterX TechnologiesInterX Technologies – FDA Inspection, Jun 3, 2016
Record Details
This FDA Inspection record concerns InterX Technologies, with an inspection on June 3, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- InterX Technologies
- Inspection Date
- June 3, 2016
- Product Type
- Devices
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ID · f8d5fb64-7a65-4638-8668-da90a5d59677
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 975150
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
5- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.30(e)Design review - Lack of or inadequate procedures
- 21 CFR 820.30(g)Design validation- Lack of or inadequate procedures
- 21 CFR 820.30(f)Design verification - documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of InterX Technologies
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 25, 2025 | Not classified | Dallas District Office | |
| November 22, 2022 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 13, 2020 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 5, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for InterX Technologies
- FDA Inspection 1277086 - 2025-07-25
- FDA Inspection 1192346 - 2022-11-22
- FDA Inspection 1120592 - 2020-02-13
- FDA Inspection 760495 - 2012-01-05
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