FDA inspection

Omni Manufacturing Services S.A. de C.V.: FDA inspection ending Jun 28, 2018

FDA inspection 1057263 · No Action Indicated (NAI) · Santa Rosa Jauregui

Key facts

Inspection ID 1057263
Firm Omni Manufacturing Services S.A. de C.V.
FEI number 3010047442
Address La Noria Lt 13 Mza 125 Parque Industrial, Calle Queretaro Rosa Jauregui; Queretaro
City Santa Rosa Jauregui
Country Mexico
Fiscal year 2018
Inspection end date Jun 28, 2018
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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