Home » French API Maker Rapped For Poor Facility Conditions
French API Maker Rapped For Poor Facility Conditions
French active pharmaceutical ingredient (API) maker Produits Chimiques Auxiliaires et de Synthese received a Form 483 for chipped paint and other deteriorating conditions in the manufacturing area of the company’s Limay, France, facility. During a June inspection, FDA investigators found unsanitary conditions near the main processing areas, including two “unclean, damaged” overhead lights above finished product drums, the form reads.
Drug GMP Report
Drug GMP Report
Upcoming Events
-
25Apr
-
07May
-
14May
-
30May