OLAAX International

FDA Regulatory Profile

OLAAX International appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-600-2013, Class I) was initiated on February 12, 2013.

Summary

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

Recent Recalls

NumberClassProductDate
D-600-2013Class IMAXILOSS Weight Advanced, 225 mg proprietary blend of herbs, supplied in 36 count capsules in Green February 12, 2013