FDA inspection

Aesculap Inc: FDA inspection ending May 5, 2015

FDA inspection 924973 · No Action Indicated (NAI) · Center Valley, PA

Key facts

Inspection ID 924973
Firm Aesculap Inc
FEI number 2916714
Address 3773 Corporate Pkwy
City Center Valley
State PA
ZIP 18034
Country United States
Fiscal year 2015
Inspection end date May 5, 2015
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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