BRIEF-Fagron Update On Fda Communication Regarding 2025 Inspection

- Fagron NV FAGRO.BR:

  • COMPANY RECEIVED A WARNING LETTER FROM FDA ON MAY 12, 2026 ASSOCIATED WITH DRUG PRODUCTS PRODUCED AT FACILITY USING IV BAGS SUPPLIED BY A THIRD-PARTY MANUFACTURER

  • PRODUCTION AT BOSTON FACILITY CONTINUES AS NORMAL, CONTINUES TO SUPPLY ITS CUSTOMERS WITH NO MATERIAL IMPACT ON BUSINESS

  • COMPREHENSIVE REMEDIATION PLAN IS IN PLACE, THE COMPANY WILL RESPOND IN FULL TO THE WARNING LETTER WITHIN THE TIMEFRAME SET OUT BY THE FDA

  • SUPPLIER HAS IMPLEMENTED CORRECTIVE ACTIONS

  • HAS NOT IDENTIFIED ANY FURTHER RELATED DEFECTS THROUGH ITS INCOMING INSPECTION REGIME

Source text: ID:nNDL38zHmL

Further company coverage: FAGRO.BR