FDA Inspection 1102948 — Nubratori, Inc

Nubratori, Inc — FEI 3010166491

The FDA completed an inspection of Nubratori, Inc on Sep 26, 2019 in Torrance, CA. 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). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 26, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Torrance, CA (United States)

Citations

IDCFRDescription
145121 CFR 211.113(b)Procedures for sterile drug products
21284FDCA 501(a)(2)(A)Disinfectant contact time

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