LGM Pharma LLC

FDA Regulatory Profile

LGM Pharma LLC appears in FDA public data with 2 recalls, 0 510(k) clearances, 5 FDA inspections, and 1 compliance action on record. Its most recent recall (D-0486-2019, Class II) was initiated on December 18, 2018.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
5
Compliance Actions
1

Recent Recalls

NumberClassProductDate
D-0486-2019Class IICIDOFOVIR DIHYDRATE, (Non-Sterile, For Manufacturing Use), 10g, Rx only, ALP PHARM BEIJING CO., LTD,December 18, 2018
D-0296-2019Class IIThyroid Powder, USP, 25kg/drum, Rx Only, Sichuan Friendly Pharmaceutical Co., LTD. NDC: 070870-1701-August 24, 2018