FDA Inspection 570578 — Acusphere, Incorporated

Acusphere, Incorporated — FEI 3004553687

The FDA completed an inspection of Acusphere, Incorporated on Feb 23, 2009 in Watertown, MA. 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 23, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Watertown, MA (United States)

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