FDA inspection

Philips Medizin Systeme Boeblingen Gmbh: FDA inspection ending Oct 18, 2006

FDA inspection 448907 · No Action Indicated (NAI) · Boblingen

Key facts

Inspection ID 448907
Firm Philips Medizin Systeme Boeblingen Gmbh
FEI number 3002807167
Address Hewlett-Packard-Str. 2
City Boblingen
Fiscal year 2007
Inspection end date Oct 18, 2006
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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