# FDA Inspection 1262940 - AMMD Labs, LLC - March 06, 2025

Source: https://www.keypedia.com/records/fda_inspections/ammd-labs-llc/6001e901-88c8-463d-934c-1da44c3e4a77
Source feed: FDA_Inspections

> FDA Inspection 1262940 for AMMD Labs, LLC on March 06, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1262940
- Company Name: AMMD Labs, LLC
- Inspection Date: 2025-03-06
- 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 1262940 - 2025-03-06](https://www.keypedia.com/records/fda_inspections/ammd-labs-llc/5144582d-9307-4273-b7f9-e1c64f17f0a3)
- [FDA Inspection 1065595 - 2018-09-14](https://www.keypedia.com/records/fda_inspections/ammd-labs-llc/ada40184-ad1f-44d5-9c29-dd9fe7240971)

Company: https://www.keypedia.com/companies/ammd-labs-llc/9a23b85b-db1e-472f-a3f4-71a457232386

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