FDA inspection

Procter & Gamble Manufacturing Mexico, S. de R.L. de C.V.: FDA inspection ending Mar 6, 2015

FDA inspection 922870 · No Action Indicated (NAI) · Naucalpan

Key facts

Inspection ID 922870
Firm Procter & Gamble Manufacturing Mexico, S. de R.L. de C.V.
FEI number 3002744909
Address San Andres Atoto No. 326, San Francisco Cuautlalpan
City Naucalpan
Country Mexico
Fiscal year 2015
Inspection end date Mar 6, 2015
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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