FDA inspection

The Procter & Gamble Manufacturing Company: FDA inspection ending May 18, 2010

FDA inspection 662272 · No Action Indicated (NAI) · Iowa City, IA

Key facts

Inspection ID 662272
Firm The Procter & Gamble Manufacturing Company
FEI number 1913771
Address 2200 Lower Muscatine Rd
City Iowa City
State IA
ZIP 52240
Country United States
Fiscal year 2010
Inspection end date May 18, 2010
Classification No Action Indicated (NAI)
Project area Colors and Cosmetics Technology
Product type Food/Cosmetics

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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

Browse all FDA inspections