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PROCEDURE The test might be carried out either in five initial containers if adequate volume of merchandise is out there in each container and the product container may be entered aseptically (i.e., needle and syringe by an elastomeric rubber stopper), or in five sterile, capped bacteriological containers of ideal dimension into which a ample quant

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Lower temperatures may be satisfactory, furnished the producer has adequate info to reveal that a decrease temperature is effective as intended.Important cookies are Definitely important for the web site to operate correctly. This category only contains cookies that ensures simple functionalities and security measures of the website. These cookies

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