GMP Laboratories of America Inc

FDA Regulatory Profile

GMP Laboratories of America Inc appears in FDA public data with 3 recalls, 0 510(k) clearances, 7 FDA inspections, and 0 compliance actions on record. Its most recent recall (H-0448-2025, Class III) was initiated on June 24, 2025.

Summary

Total Recalls
3
510(k) Clearances
0
Inspections
7
Compliance Actions
0

Recent Recalls

NumberClassProductDate
H-0448-2025Class IIILithium Orotate, Weyland Brain Nutrition ; 60 vegetarian capsules, Dietary Supplement; Distributed bJune 24, 2025
H-0447-2025Class IIILithium Orotate 2.5; 60 vegetarian capsules, Dietary Supplement; Distributed by Mecene LLC. 447 SuttJune 24, 2025
F-2297-2012Class IIDietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living herbalDecember 8, 2009