FDA inspection

Bayer de Mexico, S.A. de C.V.: FDA inspection ending Oct 23, 2015

FDA inspection 948453 · Voluntary Action Indicated (VAI) · Lerma

Key facts

Inspection ID 948453
Firm Bayer de Mexico, S.A. de C.V.
FEI number 3002806479
Address Carretera Mexico-Toluca Km. 52.5
City Lerma
Country Mexico
Fiscal year 2016
Inspection end date Oct 23, 2015
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • 1–9 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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