FDA Inspection 747510 — Henry Thayer Co

Henry Thayer Co — FEI 3008509865

The FDA completed an inspection of Henry Thayer Co on Sep 26, 2011 in Weston, CT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 26, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Weston, CT (United States)