Aribex Inc
Aribex Inc appears in FDA public data with 2 recalls, 4 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-2717-2016, Class II) was initiated on July 18, 2016. Its most recent 510(k) clearance was granted on November 16, 2017.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 4
- Inspections
- 1
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| Z-2717-2016 | Class II | NOMAD Pro2 Packaged X-Ray System, Part Number 08500021; NOMAD Pro2 Packaged X-Ray System Black, Part | July 18, 2016 |
| Z-2716-2016 | Class II | NOMAD Pro Packaged X-Ray System, Part Number 08500009; NOMAD Pro Vet Packaged X-Ray System, Part Num | July 18, 2016 |