Duy Drugs Inc.
Duy Drugs Inc. appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (F-3356-2017, Class II) was initiated on July 21, 2017.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 0
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|---|---|---|
| F-3356-2017 | Class II | Cardiovid Plus, Cardiovascular Active Dietary Supplement, 60 Softgels | July 21, 2017 |
| F-3355-2017 | Class II | Viva ben Femenine Supplement, Dietary Supplement 30 Softgels | July 21, 2017 |