FDA inspection

BUHLMANN Laboratories AG: FDA inspection ending Aug 19, 2010

FDA inspection 679136 · Official Action Indicated (OAI) · Schonenbuch

Key facts

Inspection ID 679136
Firm BUHLMANN Laboratories AG
FEI number 1000191380
Address Baselstrasse 55
City Schonenbuch
Country Switzerland
Fiscal year 2010
Inspection end date Aug 19, 2010
Classification Official Action Indicated (OAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • 1–9 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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