FDA inspection

LILMO Ltd.: FDA inspection ending Sep 12, 2018

FDA inspection 1066964 · No Action Indicated (NAI) · Pamplemousses

Key facts

Inspection ID 1066964
Firm LILMO Ltd.
FEI number 3010872792
Address Route Royale, Canton Bel Eau
City Pamplemousses
Country Mauritius
Fiscal year 2018
Inspection end date Sep 12, 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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