Celera Corporation

FDA Regulatory Profile

Celera Corporation appears in FDA public data with 1 recall, 0 510(k) clearances, 4 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-2096-2013, Class III) was initiated on July 12, 2013.

Summary

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

Recent Recalls

NumberClassProductDate
Z-2096-2013Class IIIOLA Buffer For Laboratory Use; Contents: 1 tube with buffered solution containing MgCl2 (80 ¿M) July 12, 2013