FDA Inspection 1237580 — Solevy Co. LLC

Solevy Co. LLC — FEI 3016842367

The FDA completed an inspection of Solevy Co. LLC on May 3, 2024 in Valencia, 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). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 3, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Valencia, CA (United States)

Citations

IDCFRDescription
136121 CFR 211.100(a)Absence of Written Procedures
188521 CFR 211.165(b)Microbiological testing
356721 CFR 211.84(d)(2)Component identification test