Stiefel Laboratories, Inc.
Stiefel Laboratories, Inc. appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 19, 2005.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K041342 | IMPRUV A.I. CREAM WOUND AND SKIN EMULSION | July 19, 2005 |