FDA Inspection 1327502 — Moss Tubes Inc.
The FDA completed an inspection of Moss Tubes Inc. on Jul 23, 2026 in Castleton On Hudson, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jul 23, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Castleton On Hudson, NY (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 23087 | ISO 13485:2016 Clause 7.1 | Product realization risk management processes not documented |
| 23155 | ISO 13485:2016 Clause 7.5.1 | Production and service provision not adequate |
| 23214 | ISO 13485:2016 Clause 8.2.2 | Complaint handling procedures not documented |