FDA Inspection 730835 — Alera Technologies, Inc.

Alera Technologies, Inc. — FEI 1719112

The FDA completed an inspection of Alera Technologies, Inc. on June 10, 2011 in Salt Lake City, UT. 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
June 10, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Salt Lake City, UT (United States)