ASTRA ZENECA Lp

FDA Regulatory Profile

ASTRA ZENECA Lp 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 (D-1410-2012, Class III) was initiated on July 2, 2012.

Summary

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

Recent Recalls

NumberClassProductDate
D-1410-2012Class IIINexium (esomeprazole magnesium) Delayed-Release Capsules, 40 mg, 1000-count bottle, Rx only, ManufacJuly 2, 2012