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GMP

cGMP violations dietary supplement manufacturing infographic showing 46% increase in FDA 483 observations from 2023 to 2024, 33% of facilities cited for specification failures, 600 FY2024 inspections covering approximately 5% of 13,000-15,000 registered facilities, based on FDA data and FOIA records.
August 12, 2025
by VelSafe Editorial Team Insights

cGMP Violations in Dietary Supplement Manufacturing: 40+ Statistics Through 2025-26

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Quality assurance manager reviewing FDA Part 111 GMP records and batch documentation for dietary supplement manufacturing compliance
August 10, 2025
by VelSafe Editorial Team Law

GMP Record Retention Laws for Dietary Supplement Companies: What 21 CFR Part 111 Requires

LAW: Dietary Supplement Manufacturing and Quality Compliance GMP Record Retention Laws for Dietary Supplement CompaniesWhat 21 CFR Part 111 Requires You to Keep and for How Long Record retention under 21 CFR Part 111 is not a filing preferenc

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