# FDA Inspection 1280218 - Banister Tool, Inc - August 21, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/banister-tool-inc/23fe5975-a86e-43a7-939f-148974511dc0
Source feed: FDA_Inspections

> FDA Inspection 1280218 for Banister Tool, Inc on August 21, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280218
- Company Name: Banister Tool, Inc
- Inspection Date: 2025-08-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1280218 - 2025-08-21](https://www.globalkeysolutions.net/records/fda_inspections/banister-tool-inc/2355b726-24d2-4cea-bde6-1f5098230e25)
- [FDA Inspection 1280218 - 2025-08-21](https://www.globalkeysolutions.net/records/fda_inspections/banister-tool-inc/da7db77f-14a9-4cb0-bf86-3d963bffc980)
- [FDA Inspection 885273 - 2014-06-12](https://www.globalkeysolutions.net/records/fda_inspections/banister-tool-inc/51f6a98b-627f-46b2-8d2a-2950de611131)
- [FDA Inspection 885273 - 2014-06-12](https://www.globalkeysolutions.net/records/fda_inspections/banister-tool-inc/d30af210-4f0c-42a1-b349-7c86515a52f6)

Company: https://www.globalkeysolutions.net/companies/banister-tool-inc/25c4727d-6eac-4c82-bd24-843466a5af91

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