FDA inspection

Medicoplast Co Gmbh: FDA inspection ending Feb 14, 2001

FDA inspection 65322 · No Action Indicated (NAI) · Illingen

Key facts

Inspection ID 65322
Firm Medicoplast Co Gmbh
FEI number 3002807584
Address Heusweiler Strasse 100
City Illingen
Fiscal year 2001
Inspection end date Feb 14, 2001
Classification No Action Indicated (NAI)
Project area Compliance: Med Devices
Product type Devices

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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