Avalon Packaging

FDA Regulatory Profile

Avalon Packaging appears in FDA public data with 1 recall — including 1 Class I (most serious) —, 0 510(k) clearances, 4 FDA inspections, and 1 compliance action on record. Its most recent recall (F-0996-2018, Class I) was initiated on March 9, 2018.

Summary

Total Recalls
1 (1 Class I)
510(k) Clearances
0
Inspections
4
Compliance Actions
1

Recent Recalls

NumberClassProductDate
F-0996-2018Class INXTGEN Botanicals, Maeng Da Kratom, Dietary Supplement, 70 Capsules, Made in the U.S.AMarch 9, 2018