FDA inspection

ENESTIA BELGIUM NV (SHARP BELGIUM): FDA inspection ending Dec 15, 2017

FDA inspection 1039417 · No Action Indicated (NAI) · Hamont-Achel

Key facts

Inspection ID 1039417
Firm ENESTIA BELGIUM NV (SHARP BELGIUM)
FEI number 3002958688
Address Klocknerstraat 1
City Hamont-Achel
Country Belgium
Fiscal year 2018
Inspection end date Dec 15, 2017
Classification No Action Indicated (NAI)
Project area Drug Quality Assurance
Product type Drugs

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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