On 06-11-2008 the then Drugs Inspector picked up the sample of Cledomox Suspension in Powder form Batch No.0808007, manufactured in March, 2008 by the 1st petitioner firm with expiry date as August, 2009 from M/s.Srinivasa Medical and General Stores, Kanakamahalaxmi Nagar, Visakhapatnam (listed witness No.3). The necessary formalities were complied with. The sample was sent to the Government Analyst, Drugs Control Laboratory, Hyderabad, on 07-11-2008. Report was issued to the effect that the sample was not that of standard quality. The samples does not comply in respect of Assay of Clavulanic Acid as per USP as it contain 11.65 mg/5 ml. instead of 28.5 mg/5 ml. Notice was issued to the listed witness No.3 and ultimately it was found that the drug was manufactured by A.1 firm and supplied to A.6, who is M/s.Sai Venkataramana Pharma, Bholakpur, Musheerabad, Secunderabad. After obtaining the requisite papers, the Drugs Inspector filed a charge-sheet on the file of the Chief Metropolitan Magistrate, Visakhapatnam, alleging offences punishable under Sections 18(B)(d) read with Section