Paa Laboratories Inc

FDA Regulatory Profile

Paa Laboratories Inc appears in FDA public data with 1 recall, 0 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent recall (Z-1735-2013, Class II) was initiated on April 12, 2013.

Summary

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

Recent Recalls

NumberClassProductDate
Z-1735-2013Class IIVarious types of Fetal Bovine Serum Bovine sourced Animal Sera for in-vitro diagnostic device andApril 12, 2013