FDA inspection

ALK-Abello, Inc.: FDA inspection ending Mar 1, 2019

FDA inspection 1080880 · Official Action Indicated (OAI) · Plainville, CT

Key facts

Inspection ID 1080880
Firm ALK-Abello, Inc.
FEI number 3006900385
Address 10 Farmington Valley Dr Ste 106
City Plainville
State CT
ZIP 06062
Country United States
Fiscal year 2019
Inspection end date Mar 1, 2019
Classification Official Action Indicated (OAI)
Project area Drug Quality Assurance
Product type Drugs
Warning letter 578557

At a glance

  • 10–99 Citations
  • 1–9 Posted citations
  • Yes Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 10–99 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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