Arjo, Inc.
Arjo, Inc. appears in FDA public data with 0 recalls, 1 510(k) clearance, 3 FDA inspections, and 1 compliance action on record. Its most recent 510(k) clearance was granted on May 1, 2000.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 3
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K001079 | RECUMBENT BATHING SYSTEMS, RHAPSODY AND PRIMO | May 1, 2000 |