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cGMP Audit Results: Dovita Achieves Zero Deficiency Rating for Third Consecutive Year

May 18, 2026
cGMP Audit Results: Dovita Achieves Zero Deficiency Rating for Third Consecutive Year

Our U.S. manufacturing facility passed the annual cGMP compliance audit with zero deficiencies for the third consecutive year, demonstrating our unwavering commitment to quality and regulatory compliance.

What This Means for Our Partners

- **Consistent Quality**: Zero deficiencies means every aspect of our manufacturing process meets or exceeds FDA requirements

Audit Coverage

The cGMP audit covers all dosage forms produced at our facility:

Key Audit Areas

1. Facility cleanliness and maintenance

This achievement reflects the dedication of our entire team and our investment in continuous improvement.

Frequently Asked Questions

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