Syntec Pharma Corp

FDA Regulatory Profile

Syntec Pharma Corp 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 (D-0014-2019, Class II) was initiated on August 22, 2018.

Summary

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

Recent Recalls

NumberClassProductDate
D-0014-2019Class IITHYROID POWDER USP (Levothyroxine labeled range of 34.2-41.8mcg/grain; Liothyroine (correct spellingAugust 22, 2018
D-0013-2019Class IITHYROID POWDER USP, Full Strength (Levothyroxine labeled range of 103-125mcg/grain; Liothyroine (corAugust 22, 2018