Nuway Distributors, LLC

FDA Regulatory Profile

Nuway Distributors, LLC 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-0667-2016, Class I) was initiated on December 23, 2015.

Summary

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

Recent Recalls

NumberClassProductDate
D-0667-2016Class IAPEXXX tablets, 300 mg, packaged in 1-count blister cards, Distributed Exclusively by: Nuway DistribDecember 23, 2015