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AAF stands committed to build world class products for its respective market. India is a major manufacturing hub for pharmaceutical manufacturing for India as well as USA and other export markets. The cleanroom classification calls for a leak free HEPA filer every time it is validated.
A test confirming to site test protocol as per EN1822 is a must. EN1822 require full filter auto scan testing in the factory. AAF India has shown its commitment by investing in an auto scan filter test machine to ensure each one of the HEPA/ULPA filter confirms to specific test requirement of EN1822and test it at MPPS.
