No Written Observations by the FDA during the audit of the Zingonia site
The US Food & Drug Administration recently audited the Zingonia Food Supplement manufacturing site of Fine Foods. No FDA 483 form was issued, meaning that no written observations were received, a further evidence of the commitment of Fine Foods to the quality of the products manufactured in its plants. The Zingonia site by the implementation of the GMPs and HACCP risk analysis, has developed a solid food safety management system certified ISO 22000 with the purpose to take under control food safety hazards. Quality System consequently ensures that Fine Foods products are in compliance with the release specifications and safe for the consumer.