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FDA Inspection 1277866 — Aesculap Inc

Aesculap Inc — FEI 2916714

The FDA completed an inspection of Aesculap Inc on July 11, 2025 in Center Valley, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 11, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Center Valley, PA (United States)

Facility

Other inspections at this facility

  • 1148504 (VAI Wed Aug 11 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 977569 (NAI Wed Jul 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 924973 (NAI Tue May 05 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 828602 (NAI Wed Apr 24 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 822299 (VAI Tue Mar 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources