Food · Food Safety · Intermediate
Complete within 24 hours of any deviation from a preventive control. PCQI must review all corrective action records. Retain for at least 2 years.
A corrective action documentation log for food safety teams recording deviations from preventive controls under the FDA Food Safety Modernization Act. Captures the deviation details, affected product identification and disposition, root cause analysis, corrective measures taken, and PCQI verification — the complete record required by 21 CFR Part 117 Subpart F.
FSMA requires that corrective actions address the food safety problem, evaluate affected food for safety, and prevent recurrence. FDA inspectors review corrective action records to verify the facility's food safety system is functioning. This log provides the structured documentation that satisfies those record requirements.
This checklist template is provided as a general-purpose resource and is not tailored to the regulatory requirements of any specific country, region, or jurisdiction. It is the responsibility of each organisation to review and adapt this template to ensure compliance with all applicable local laws and regulations. Miratag does not accept liability for any inaccuracies or omissions, or for any actions taken based on this template.
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