FDA Inspection 648165 — Neos Therapeutics, LP

Neos Therapeutics, LP — FEI 3000205839

The FDA completed an inspection of Neos Therapeutics, LP on February 26, 2010 in Grand Prairie, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 26, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Grand Prairie, TX (United States)