Duties of Inspectors specially authorised to inspect the manufacture of Ayurvedic

Subject to the instructions of the controlling authority, it shall be the duty of an Inspector authorised to inspect the manufacture of Ayurvedic (including Siddha) or Unani drugs– (i) to inspect not less than twice a year, all premises licensed for manufacture of Ayurvedic (including Siddha) or Unani drugs within the area allotted to him and to satisfy himself that the conditions of the licence and the provisions of the Act and the rules made thereunder are being observed; (ii) to send forthwith to the controlling authority after each inspection a detailed report indicating whether or not the conditions of the licence and the provisions of the Act and the rules made thereunder are being observed; (iii) to take samples of the drugs manufactured on the premises and send them for test or analysis in accordance with these rules; (iv) to institute prosecutions in respect of violation of the Act and the Rules made thereunder.