FDA Inspection
QuVa Pharma, Inc.QuVa Pharma, Inc. – FDA Inspection, Jun 2, 2017
Record Details
This FDA Inspection record concerns QuVa Pharma, Inc., with an inspection on June 2, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · e07d3c56-3f07-4db6-819c-bc6b04f5d745
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1012820
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 211.113(b)Procedures for sterile drug products
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Other FDA inspections of QuVa Pharma, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 4, 2026 | Not classified | Dallas District Office | Drug Quality Assurance |
| October 28, 2024 | VAI | Dallas District Office | Drug Quality Assurance |
| August 18, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 23, 2019 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 8, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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