We are able to provide you with a large number of different compliance documents with analyzed results made for each specific material according to FDA § 21 CFR 177.

These documents are based on the processes at Accofluor and information from our supplier of raw materials. Accofluor compresses and anneals the compounds within the supplier’s recommendations, and turn out parts without adding ingredients or using agents/coolants.

Traceability is kept in compliance with regulation 2023/2006 (GMP).