# FDA Inspection 1276112 - Centerline Biomedical Inc - July 02, 2025

Source: https://www.keypedia.com/records/fda_inspections/centerline-biomedical-inc/b9b9a538-f80b-4fba-9501-a7ddcd4ecfc5
Source feed: FDA_Inspections

> FDA Inspection 1276112 for Centerline Biomedical Inc on July 02, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1276112
- Company Name: Centerline Biomedical Inc
- Inspection Date: 2025-07-02
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1276112 - 2025-07-02](https://www.keypedia.com/records/fda_inspections/centerline-biomedical-inc/69544bfb-4698-4330-88c7-f10802f3961a)
- [FDA Inspection 1276112 - 2025-07-02](https://www.keypedia.com/records/fda_inspections/centerline-biomedical-inc/8911e73f-56f1-4ee5-a281-974eadaf2b01)

Company: https://www.keypedia.com/companies/centerline-biomedical-inc/8fec59a7-69b8-41b8-ae3f-fa965e839ff8

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