FDA inspection

Fersinsa GB, SA de CV: FDA inspection ending Jan 19, 2009

FDA inspection 571583 · Voluntary Action Indicated (VAI) · Ramos Arizpe

Key facts

Inspection ID 571583
Firm Fersinsa GB, SA de CV
FEI number 3000538793
Address Planta Sintesis, Camino A Guanajuato S/N
City Ramos Arizpe
Country Mexico
Fiscal year 2009
Inspection end date Jan 19, 2009
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None 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

Browse all FDA inspections