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FDA inspection

Coloplast Manufacturing US, LLC: FDA inspection ending Feb 11, 2000

FDA inspection 14581 · Voluntary Action Indicated (VAI) · North Mankato, MN

Key facts

Inspection ID 14581
Firm Coloplast Manufacturing US, LLC
FEI number 2125337
Address 1940 Commerce Dr
City North Mankato
State MN
ZIP 56003-1700
Fiscal year 2000
Inspection end date Feb 11, 2000
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation|OTC Drug Evaluation
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes 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.

Other inspections at this establishment

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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