FDA Inspection
Moss Tubes Inc.Moss Tubes Inc. – FDA Inspection, Jul 23, 2026
Record Details
This FDA Inspection record concerns Moss Tubes Inc., with an inspection on July 23, 2026, issued by the Center for Devices and Radiological Health, covering devices.
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ID · f626abef-6f84-421d-984a-52d1199ccdbd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1327502
- Project area
- Compliance: Devices
FDA Citations
3- ISO 13485:2016 Clause 7.1Product realization risk management processes not documented
- ISO 13485:2016 Clause 8.2.2Complaint handling procedures not documented
- ISO 13485:2016 Clause 7.5.1Production and service provision not adequate
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Other FDA inspections of Moss Tubes Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 13, 2021 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 12, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 12, 2015 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 21, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Moss Tubes Inc.
- FDA Inspection 1149249 - 2021-08-13
- FDA Inspection 1030997 - 2017-05-12
- FDA Inspection 950519 - 2015-11-12
- FDA Inspection 799519 - 2012-09-21
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