FDA inspection

The Procter & Gamble Manufacturing Company: FDA inspection ending Sep 27, 2024

FDA inspection 1252187 · No Action Indicated (NAI) · Iowa City, IA

Key facts

Inspection ID 1252187
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 2024
Inspection end date Sep 27, 2024
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
  • 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

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