FDA Inspection 648326 — NEXAIR, LLC

NEXAIR, LLC — FEI 3003329108

The FDA completed an inspection of NEXAIR, LLC on Feb 25, 2010 in Jacksonville, FL. 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
Feb 25, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jacksonville, FL (United States)

Citations

IDCFRDescription
188321 CFR 211.165(a)Testing and release for distribution