FDA Inspection
Netech Corp.Netech Corp. – FDA Inspection, May 24, 2012
Record Details
This FDA Inspection record concerns Netech Corp., with an inspection on May 24, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Netech Corp.
- Inspection Date
- May 24, 2012
- Product Type
- Devices
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ID · 4dc60f9b-58dc-4ce0-8c50-2fe4a413e03e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 783431
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.80(b)Incoming acceptance records, documentation
- 21 CFR 820.198(b)Review and evaluation for investigation
- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.22Quality audits - Lack of or inadequate procedures
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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 |
| October 8, 2019 | 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 |
| January 29, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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