FDA Inspection 801732 — AG Essence, Inc.

AG Essence, Inc. — FEI 3009562273

The FDA completed an inspection of AG Essence, Inc. on October 16, 2012 in Sandston, VA. 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
October 16, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sandston, VA (United States)