Food and Drug Regulations

Version of section C.04.422 from 2006-12-14 to 2014-10-22:


 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: