FDA inspection

Messer LLC: FDA inspection ending Jul 23, 2002

FDA inspection 231021 · Voluntary Action Indicated (VAI) · Claymont, DE

Key facts

Inspection ID 231021
Firm Messer LLC
FEI number 2516947
Address 6000 Philadelphia Pike,
City Claymont
State DE
ZIP 19703-2717
Fiscal year 2002
Inspection end date Jul 23, 2002
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 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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