FDA Inspection 1223353 — Aesculap Implant Systems LLC
The FDA completed an inspection of Aesculap Implant Systems LLC on Nov 9, 2023 in Breinigsville, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 9, 2023
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Breinigsville, PA (United States)