QuVa Pharma, Inc.
FDA regulatory history for QuVa Pharma, Inc.: 36 Form 483s, 38 Recalls.
36Form 483s
0Warning Letters
38Recalls
74Total Actions
Jun 24, 2026Last Event
Total Actions = Form 483s + Warning Letters + Recalls.
GMP issues cited
- Aseptic Processing (4)
- Investigations (3)
- Training Competency (2)
- Equipment Qualification (2)
- Labeling Controls (1)
Facility types: Biologics, Pharmaceutical
See the regulatory timeline, risk score, GMP issue radar, peer comparison, and document downloads on the 483 Signal dashboard.
This profile aggregates publicly available FDA documents and does not constitute an assessment of this company's compliance status. Companies may have taken corrective actions not yet reflected in public records. Provided for informational purposes only.