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FDA Inspection 1223353 — Aesculap Implant Systems LLC

Aesculap Implant Systems LLC — FEI 3005739625

The FDA completed an inspection of Aesculap Implant Systems LLC on November 9, 2023 in Breinigsville, 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
November 9, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Breinigsville, PA (United States)

Facility

Other inspections at this facility

  • 1143458 (VAI Tue Jun 08 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 916478 (VAI Wed Mar 04 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 796358 (NAI Mon Aug 27 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources