FDA inspection

Teva Pharmaceuticals USA dba Copley Manufacturing: FDA inspection ending Nov 10, 2005

FDA inspection 401800 · No Action Indicated (NAI) · South Boston, MA

Key facts

Inspection ID 401800
Firm Teva Pharmaceuticals USA dba Copley Manufacturing
FEI number 1250024
Address 79 Dresser St
City South Boston
State MA
ZIP 02127-1337
Fiscal year 2006
Inspection end date Nov 10, 2005
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
  • Yes 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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