FDA Inspection 1042033 — Guy & O'Neill Inc.

Guy & O'Neill Inc. — FEI 3010164716

The FDA completed an inspection of Guy & O'Neill Inc. on February 20, 2018 in Fredonia, WI. 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 20, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fredonia, WI (United States)