FDA inspection

Leica Instruments (Singapore) Pte., Ltd.: FDA inspection ending Jul 1, 2016

FDA inspection 987547 · No Action Indicated (NAI) · Singapore South West

Key facts

Inspection ID 987547
Firm Leica Instruments (Singapore) Pte., Ltd.
FEI number 1000204638
Address 12 Teban Gardens Crescent
City Singapore South West
Country Singapore
Fiscal year 2016
Inspection end date Jul 1, 2016
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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