# FDA Inspection 1280950 - Armadillo Additive Inc - August 13, 2025

Source: https://www.keypedia.com/records/fda_inspections/armadillo-additive-inc/9f6dfeaa-53dd-47d2-a3de-e5c2378e3b66
Source feed: FDA_Inspections

> FDA Inspection 1280950 for Armadillo Additive Inc on August 13, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280950
- Company Name: Armadillo Additive Inc
- Inspection Date: 2025-08-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1280950 - 2025-08-13](https://www.keypedia.com/records/fda_inspections/armadillo-additive-inc/70a97f72-93b1-4c1b-8d86-4cd67d43e566)
- [FDA Inspection 1280950 - 2025-08-13](https://www.keypedia.com/records/fda_inspections/armadillo-additive-inc/e50bbfb4-4660-4f81-8d38-a246f04c652e)

Company: https://www.keypedia.com/companies/armadillo-additive-inc/d1816aae-c718-4892-9b15-934e398f3f86

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