China NMPA Product Recall - Pulsed arteriovenous pneumatic compression therapy device
China NMPA product recall for Pulsed arteriovenous pneumatic compression therapy device by Anhui Aerospace Biotechnology Co., Ltd. published August 29, 2017. Recall level: Level 3 Recall. Anhui Aerospace Biotechnology Co., Ltd. initiated a voluntary Class III recall of its Pulsating Arte
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China NMPA product recall for Pulsed arteriovenous pneumatic compression therapy device by Anhui Aerospace Biotechnology Co., Ltd. published August 29, 2017. Recall level: Level 3 Recall. Anhui Aerospace Biotechnology Co., Ltd. initiated a voluntary Class III recall of its Pulsating Arte
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