FDA Inspection 1328388 — Lear Corporation (AccuMed)
The FDA completed an inspection of Lear Corporation (AccuMed) on Jul 28, 2026 in Pine Grove, 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
- Jul 28, 2026
- Fiscal Year
- 2026
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Pine Grove, PA (United States)