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TPI > SEC Filings for TPI > Form 8-K/A on 8-Jul-2014All Recent SEC Filings




Other Events

Item 8.01. Other Events

On April 7, 2014, Tianyin Pharmaceutical Inc. (the "Company" or "TPI") filed a Current Report on Form 8-K (the "Form 8-k") regarding the examination for quality and pricing tests that were conducted by the CFDA of Sichuan province on the Company, which resulted in the Company's Good Manufacturing Practice ("GMP") certificate being administered by the provincial CFDA and, that as a result, production and sale of certain of the Company's products were temporarily halted, pending the results of quality and pricing tests.

On May 14, 2014, the Company filed an amendment to the Form 8-K to announce that on May 9, 2014 the Company received its renewed GMP certificate for both of its Chengdu Tianyin's pre-extraction facility in the city of Chengdu and formulation facility at Longquan County of Chengdu, valid until the end of 2015. Normal manufacturing and sales for most of the Company's products resumed, except the tablets formulation division which was scheduled to be further inspected for its production process by the provincial CFDA staff on May 24, 2014. On June 23, 2014, the Company filed a second amendment to the Form 8-K to announce that the Company passed the inspection on its tablets formulation division and was waiting to receive the relevant GMP certificate.

The Company is filing this amendment to the Form 8-K to announce that on July 3, 2014 the Company received the relevant GMP certificate for the tablets formulation division issued by the CFDA of Sichuan province on June 20, 2014.

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