FDA inspection

Microtek Medical Malta Limited: FDA inspection ending May 31, 2018

FDA inspection 1058607 · No Action Indicated (NAI) · Il-Mosta

Key facts

Inspection ID 1058607
Firm Microtek Medical Malta Limited
FEI number 3006581049
Address Sorbonne Centre F20, 5 Techno Park
City Il-Mosta
Country Malta
Fiscal year 2018
Inspection end date May 31, 2018
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

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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