Actelion Pharmaceuticals U.S., Inc.

FDA Regulatory Profile

Actelion Pharmaceuticals U.S., Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-143-2013, Class III) was initiated on January 16, 2013.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-143-2013Class IIIVentavis (iloprost) Inhalation Solution, 10 mcg/1 mL, Sterile, 30 Single Use Ampules per carton, ManJanuary 16, 2013