# FDA Inspection 1328388 - Lear Corporation (AccuMed) - July 28, 2026

Source: https://www.keypedia.com/records/fda_inspections/lear-corporation-accumed/7f075e88-6af1-44a9-b511-4ccdea1f57db
Source feed: FDA_Inspections

> FDA Inspection 1328388 for Lear Corporation (AccuMed) on July 28, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1328388
- Company Name: Lear Corporation (AccuMed)
- Inspection Date: 2026-07-28
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1169367 - 2022-04-25](https://www.keypedia.com/records/fda_inspections/lear-corporation-accumed/5b7015e8-151a-451f-a472-55802f7f4a15)

Company: https://www.keypedia.com/companies/lear-corporation-accumed/0b985d1b-ed75-4e9b-ad8c-a61b39eb0fb0

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7