Konsyl Pharmaceuticals Inc

FDA Regulatory Profile

Konsyl Pharmaceuticals Inc appears in FDA public data with 1 recall, 1 510(k) clearance, 3 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1315-2014, Class III) was initiated on April 1, 2014. Its most recent 510(k) clearance was granted on November 15, 2018.

Summary

Total Recalls
1
510(k) Clearances
1
Inspections
3
Compliance Actions
0

Recent Recalls

NumberClassProductDate
D-1315-2014Class IIIPSYLLIUM FIBER, Laxative/Supplement, 100 Capsules, OTC. Manufactured By: Konsyl Pharmaceuticals, InApril 1, 2014

Recent 510(k) Clearances

K-NumberDeviceDate
K181750SITZMARKSNovember 15, 2018