FDA inspection

NPA de Mexico S.A. de C.V.: FDA inspection ending May 9, 2018

FDA inspection 1056092 · No Action Indicated (NAI) · Tijuana

Key facts

Inspection ID 1056092
Firm NPA de Mexico S.A. de C.V.
FEI number 3003542872
Address Sor Juana Ines De La Cruz, Industrial # 20150 Interior 5 Cd.
City Tijuana
Fiscal year 2018
Inspection end date May 9, 2018
Classification No Action Indicated (NAI)
Project area Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood & Blood Products|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product 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Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood Products|Product Evaluation: Med Devices|Product Evaluation: Medical Devices|Blood and Blood 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Product type Biologics, Devices

At a glance

  • None Citations
  • None 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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