FDA inspection

Bemis Manufacturing Company: FDA inspection ending Aug 14, 2019

FDA inspection 1099553 · Voluntary Action Indicated (VAI) · Sheboygan Falls, WI

Key facts

Inspection ID 1099553
Firm Bemis Manufacturing Company
FEI number 3000209940
Address W2940 Old County Road Pp
City Sheboygan Falls
State WI
ZIP 53085
Country United States
Fiscal year 2019
Inspection end date Aug 14, 2019
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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