Authorisation may be suspended or withdrawn by reasoned decision of the Director General of the Agence nationale de sécurité du médicament et des produits de santé where the advertising of the medical device no longer complies with the conditions laid down by the provisions of Articles L. 5213-2 and L. 5213-4, and by the provisions of this chapter.
Suspension or withdrawal may only take place after the holder has been invited, by any means enabling the date of receipt of this notice to be proven, to present his written or oral observations within a period set by the Director General, which may not be less than one month.