Code of Maine Rules
02 - DEPARTMENT OF PROFESSIONAL AND FINANCIAL REGULATION
392 - MAINE BOARD OF PHARMACY
Part 5 - LICENSE DENIAL AND PROFESSIONAL DISCIPLINE
Chapter 34 - LICENSURE OF RETAIL SUPPLIERS OF MEDICAL OXYGEN
Section 392-5-34-8 - Compliance with Current Good Manufacturing Practices; Incorporation by Reference
Current through 2024-38, September 18, 2024
1. Current Good Manufacturing Practices
A retail supplier of medical oxygen that manufactures, processes, packages or holds oxygen as defined in the Federal Food, Drug, and Cosmetic Act and its implementing rules shall comply with the current good manufacturing practices promulgated by the Food and Drug Administration in 21 CFR Parts 210 and 211 (April 1, 2012 edition).
2. Incorporation by Reference
The board hereby incorporates the following documents by reference into this chapter:
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm
This document may also be obtained from the State Law Library, State House, Augusta, Maine, tel. (207) 287-1600.
http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm
This document may also be obtained from the State Law Library, State House, Augusta, Maine, tel. (207) 287-1600.