Mobius Therapeutics LLC

FDA Regulatory Profile

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
0
Inspections
2
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-809-2013Class IMitosol (mitomycin for solution), 0.2 mg/vial, Kit for Ophthalmic Use (NDC 49771-002-01), 3 kits perJanuary 3, 2013