FDA inspection

The Procter & Gamble Manufacturing Company: FDA inspection ending May 9, 2008

FDA inspection 518161 · No Action Indicated (NAI) · Greensboro, NC

Key facts

Inspection ID 518161
Firm The Procter & Gamble Manufacturing Company
FEI number 1017175
Address 100 S Swing Rd
City Greensboro
State NC
ZIP 27409-2006
Fiscal year 2008
Inspection end date May 9, 2008
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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