Food and Drug Regulations
Version of section C.04.422 from 2006-12-14 to 2014-10-22:
C.04.422 If a fabricator recalls source plasma for a reason involving product safety, the fabricator shall provide the Minister with a written report stating the reason for the recall, the number of units involved and the location from which the units were recalled.
- SOR/78-545, s. 1
- SOR/2006-353, s. 1
- Date modified: