GnuPharma Corp.

FDA Regulatory Profile

GnuPharma Corp. appears in FDA public data with 6 recalls, 0 510(k) clearances, 2 FDA inspections, and 1 compliance action on record. Its most recent recall (F-0301-2017, Class II) was initiated on May 8, 2017.

Summary

Total Recalls
6
510(k) Clearances
0
Inspections
2
Compliance Actions
1

Recent Recalls

NumberClassProductDate
F-0301-2017Class IIGnuPharma ECS Herbal Tea Relief SAMPLE ONLYMay 8, 2017
F-0298-2017Class IIGnuPharma Sleep 100% Herbal Supplement 60 CapsulesMay 8, 2017
F-0300-2017Class IIGnuPharma Foundation 100% Herbal Supplement 60 CapsulesMay 8, 2017
F-0299-2017Class IIGnuPharma Stress 100% Herbal Supplement 60 CapsulesMay 8, 2017
F-0296-2017Class IIGnuPharma Fit 100% Herbal Supplement 60 CapsulesMay 8, 2017
F-0297-2017Class IIGnuPharma Relief 100% Herbal Supplement 60 CapsulesMay 8, 2017