Supplement Manufacturing Partner Inc.

FDA Regulatory Profile

Supplement Manufacturing Partner Inc. appears in FDA public data with 2 recalls — including 1 Class I (most serious) —, 0 510(k) clearances, 5 FDA inspections, and 0 compliance actions on record. Its most recent recall (F-0729-2025, Class I) was initiated on April 4, 2025.

Summary

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

Recent Recalls

NumberClassProductDate
F-0729-2025Class ISpermidine, Maximum Strength, 10 mg per serving, Support healthy Aging, Dietary Supplement, 120 CapsApril 4, 2025
F-1224-2023Class IIHavasu Beetroot Powder, 11.5 oz.June 12, 2023