FDA Inspection
Netech Corp.Netech Corp. – FDA Inspection, Oct 8, 2019
Record Details
This FDA Inspection record concerns Netech Corp., with an inspection on October 8, 2019, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Netech Corp.
- Inspection Date
- October 8, 2019
- Product Type
- Devices
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ID · 657cebba-4e46-47f9-873f-5b42cee120cd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1106387
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
- 21 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements
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Other FDA inspections of Netech Corp.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 14, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 16, 2016 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 28, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 24, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 29, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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