FDA Inspection 709512 — Fresenius USA Manufacturing, Inc.

Fresenius USA Manufacturing, Inc. — FEI 1713747

The FDA completed an inspection of Fresenius USA Manufacturing, Inc. on February 4, 2011 in Ogden, 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
February 4, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ogden, UT (United States)