Audits / Assessments
TechniCAL can provide an on-site assessment of your compliance with FDA canning regulations. Either as an independent auditor or as part of your corporate audit team, TechniCAL can participate to help gauge facility compliance. Our audits are based on the most critical parts of these regulatory requirements. A complete report of our findings is provided upon completion.
FDA Style Inspection
TechniCAL’s Audits are based on the the most critical areas of the FDA canning regulatory requirements:
- Process Source Documentation
- Retort Validation Documentation
- Process Delivery
- Process Deviations
- Container Integrity
Complete Audit Report
A complete report of our findings is provided upon completion, along with suggestions on how to address any issues out of compliance. Report includes a detailed checklist of FDA Canning Regulations, showing compliance status of each item. Also includes list of observations and recommendations from TechniCAL how to address each finding.
Audit Team
TechniCAL can be part of your corporate audit team. Teams often participate in annual audits to prepare for FDA inspections, Supplier Audits, SQF Qualification, and to check internal company policies. Including TechniCAL on your team brings an independent process authority point of view, withe an eye for the critical areas of FDA canning regulations.