FDA inspection

Bemis Manufacturing Co.: FDA inspection ending Oct 31, 2007

FDA inspection 494545 · Voluntary Action Indicated (VAI) · Sheboygan Falls, WI

Key facts

Inspection ID 494545
Firm Bemis Manufacturing Co.
FEI number 3000209940
Address W2940 Old County Road Pp
City Sheboygan Falls
State WI
ZIP 53085-2528
Fiscal year 2008
Inspection end date Oct 31, 2007
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Med Devices
Product type Devices

At a glance

  • None 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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