FDA Inspection 732385 — Levlad, LLC

Levlad, LLC — FEI 1000222390

The FDA completed an inspection of Levlad, LLC on Jun 17, 2011 in Chatsworth, 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
Jun 17, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chatsworth, CA (United States)

Citations

IDCFRDescription
117721 CFR 211.63Equipment Design, Size and Location
145021 CFR 211.113(a)Procedures for non-sterile drug products
361321 CFR 211.160(b)(4)Establishment of calibration procedures