I.-Any violation observed within the Armed Forces Blood Transfusion Centre of the legislative and regulatory requirements applicable to it, as well as the elements mentioned in article L. 1222-11, may result in the modification or temporary or permanent withdrawal of the approval provided for in VI of article L. 1222-11 under the conditions mentioned in this article.
II -Modification or withdrawal may only take place after formal notice has been given to the Minister of Defence to take all appropriate measures to remedy the breach or failure observed or to provide all necessary explanations.
III -In the event of an emergency involving the safety of individuals, the Director of the Agence nationale de sécurité du médicament et des produits de santé (French National Agency for the Safety of Medicines and Health Products) will immediately inform the Minister for Defence, who will take the appropriate measures without delay.