FDA Inspection 675315 — Biodel Inc

Biodel Inc — FEI 3006578040

The FDA completed an inspection of Biodel Inc on Jul 15, 2010 in Danbury, CT. 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
Jul 15, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Danbury, CT (United States)

Additional Details

Sponsor, Contract Research Organization