FDA Inspection 1012820 — QuVa Pharma, Inc.

QuVa Pharma, Inc. — FEI 3012053582

The FDA completed an inspection of QuVa Pharma, Inc. on Jun 2, 2017 in Sugar Land, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 2, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sugar Land, TX (United States)

Citations

IDCFRDescription
145121 CFR 211.113(b)Procedures for sterile drug products

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