Spondyeze (Cancelled from the ARTG under 30(2)(a), 30(2)(ba), 30(1)(g) and 30(2)(e) of the Act)
Product name
Spondyeze
ARTG
169259
Date action takes effect
Compliance action
Complementary medicine cancellation
Type of action
Cancelled from the ARTG under 30(2)(a), 30(2)(ba), 30(1)(g) and 30(2)(e) of the Act
Grounds for regulatory action
It appeared to the Secretary that the quality, safety or efficacy of the goods was unacceptable. It appeared to the Secretary that a certification made by the sponsor under paragraph 26A(2)(b) of the Act was incorrect. The Secretary was satisfied that a statement made in, or in connection with, the application for listing of the goods was false or misleading in a material particular. The goods did not conform to a standard applicable to the goods.