FDA Inspection 1269501 — Bemis Manufacturing Company

Bemis Manufacturing Company — FEI 3000209940

The FDA completed an inspection of Bemis Manufacturing Company on April 30, 2025 in Sheboygan Falls, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 30, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Sheboygan Falls, WI (United States)