CFDA Announced the 1st Oversea Medical Device Manufacturing Sites Inspection Results

In order to strength the imported medical device post-marketing supervision, December 2^nd 2015, China Food and Drug Administration (CFDA) issued the announcement about‘ CFDA Initially Organized Oversea Medical Device Manufacturing GMP On-site Inspection'.

November 28^th 2017, it was the first time CFDA announced LABORATOIRES URGO，PRODIMED，MedTrade Products Limited，BIOKIT, S.A. and Beckman Coulter, Inc. the oversea medical device manufacturing sites inspection results.

Notice List

• The Notice for the LABORATOIRES URGO oversea medical device manufacturing sites inspection results.
• The Notice for the PRODIMED oversea medical device manufacturing sites inspection results.
• The Notice for the MedTrade Products Limited oversea medical device manufacturing sites inspection results.
• The Notice for the BIOKIT, S.A. oversea medical device manufacturing sites inspection results.
• The Notice for the Beckman Coulter, Inc. oversea medical device manufacturing sites inspection results.