{"data":{"id":"us-mt/50-33-101","jurisdiction":"us-mt","citation":"50-33-101","heading":"Labeling of containers by blood banks required.","body":"Each container or package containing any whole blood, plasma, blood products, or blood derivatives sold by a blood bank shall have plainly stamped or printed thereon the fact that the product therein was tested as required in 50-33-104, giving the date of the test and such information as is necessary to designate the type of test made.","path":["TITLE 50. HEALTH AND SAFETY","CHAPTER 33. BLOOD AND BLOOD PRODUCTS","Part 1. General Provisions"],"source_url":"https://mca.legmt.gov/bills/mca/title_0500/chapter_0330/part_0010/section_0010/0500-0330-0010-0010.html","current_through":"Montana Code Annotated 2025","vintage":"","retrieved_at":"2026-09-14T04:56:25Z","sha256":"424d6cb0fb8f9cd86d83afdb7035af86bdc1b6e322fa264ca63f9cd9d93bf154","source_id":"us-mt","stale":false,"prev":"us-mt/50-32-611","next":"us-mt/50-33-102"},"notice":"GroundRules: Original legal text. Not legal advice."}