FDA inspection

Bristol Myers Squibb Manufacturing, Co.: FDA inspection ending Jun 11, 2008

FDA inspection 523224 · No Action Indicated (NAI) · Barceloneta, PR

Key facts

Inspection ID 523224
Firm Bristol Myers Squibb Manufacturing, Co.
FEI number 2623241
Address Road # 2, Km # 56.4
City Barceloneta
State PR
ZIP 00617
Fiscal year 2008
Inspection end date Jun 11, 2008
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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