Greetings all.
Is there anyone can give me examples of root cause for Non-Compliance Findings belows:
1. No validation conducted for critical limits for both CCP 1 (receiving of raw material temperature ≤4°C) and CCP 2 (cold room storage temperature ≤-18°C). and,
2. The establishment did not maintain documented procedures for verification:
ii. End products and environment cleanliness (swab test) sampling not conducted as scheduled in year 2020.