Aptalis Pharmatech Inc.

FDA Regulatory Profile

Aptalis Pharmatech Inc. appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1006-2015, Class II) was initiated on November 13, 2014.

Summary

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

Recent Recalls

NumberClassProductDate
Z-1006-2015Class IIFLUTTER Percussor respiratory device, packaged one unit per clear plastic package. Product UsagNovember 13, 2014