FDA Inspection
Moss Tubes Inc.Moss Tubes Inc. – FDA Inspection, Nov 12, 2015
Record Details
This FDA Inspection record concerns Moss Tubes Inc., with an inspection on November 12, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Moss Tubes Inc.
- Inspection Date
- November 12, 2015
- Product Type
- Devices
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ID · d234fef6-381a-44fc-bbc8-76474960e596
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 950519
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
6- 21 CFR 803.50(b)(1)Reporting Information Reasonably Known
- 21 CFR 803.50(a)(2)Individual Report of Malfunction
- 21 CFR 803.50(a)(1)Report of Death or Serious Injury
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.22Quality Audits - defined intervals
- 21 CFR 820.50(a)(2)Supplier oversight
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Other FDA inspections of Moss Tubes Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 23, 2026 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| 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 |
| September 21, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Moss Tubes Inc.
- FDA Inspection 1327502 - 2026-07-23
- FDA Inspection 1149249 - 2021-08-13
- FDA Inspection 1030997 - 2017-05-12
- FDA Inspection 799519 - 2012-09-21
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