FDA inspection

Sterigenics Germany GmbH: FDA inspection ending Aug 17, 2000

FDA inspection 39457 · No Action Indicated (NAI) · Wiesbaden

Key facts

Inspection ID 39457
Firm Sterigenics Germany GmbH
FEI number 3006003617
Address Industrie Park Kalle-Albert, Kasteler Str. 45
City Wiesbaden
Fiscal year 2000
Inspection end date Aug 17, 2000
Classification No Action Indicated (NAI)
Project area Product Evaluation: 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
  • 10–99 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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