FDA Inspection
Moss Tubes Inc.Moss Tubes Inc. – FDA Inspection, May 12, 2017
Record Details
This FDA Inspection record concerns Moss Tubes Inc., with an inspection on May 12, 2017, issued by the Center for Devices and Radiological Health, covering devices.
View Company Profile
ID · a7dead0b-ae0f-488f-97aa-10a0310ff908
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1030997
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
- 21 CFR 820.75(a)Documentation
- 21 CFR 820.80(e)Documentation
Full citation text and observation details available on the Dashboard.
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 |
| 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 1327502 - 2026-07-23
- FDA Inspection 1149249 - 2021-08-13
- FDA Inspection 950519 - 2015-11-12
- FDA Inspection 799519 - 2012-09-21
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.