FDA Inspection 570578 — Acusphere, Incorporated

Acusphere, Incorporated — FEI 3004553687

The FDA completed an inspection of Acusphere, Incorporated on February 23, 2009 in Watertown, MA. 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 23, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Watertown, MA (United States)