Leiter's Enterprises, Inc.

FDA Regulatory Profile

Leiter's Enterprises, 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-0518-2019, Class II) was initiated on February 19, 2019.

Summary

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

Recent Recalls

NumberClassProductDate
D-0518-2019Class IICefuroxime 10 mg/mL in Sodium Chloride, Intravitreal injection, 1 mL in a 2mL Vial, Ophthalmic Use OFebruary 19, 2019