# FDA Inspection 1150920 - Medical Technology Products - September 01, 2021

Source: https://www.keypedia.com/records/fda_inspections/medical-technology-products/4d88df66-cdcd-4479-babf-99338a2decd6
Source feed: FDA_Inspections

> FDA Inspection 1150920 for Medical Technology Products on September 01, 2021. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1150920
- Company Name: Medical Technology Products
- Inspection Date: 2021-09-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1150920 - 2021-09-01](https://www.keypedia.com/records/fda_inspections/medical-technology-products/49709650-082b-463d-ba56-4eeb69561494)
- [FDA Inspection 928855 - 2015-05-01](https://www.keypedia.com/records/fda_inspections/medical-technology-products/01c21992-62ee-475b-8bb8-207725a09f44)
- [FDA Inspection 791452 - 2012-07-17](https://www.keypedia.com/records/fda_inspections/medical-technology-products/587a23e8-ed75-4e97-8600-e53a50f21488)
- [FDA Inspection 638786 - 2010-01-12](https://www.keypedia.com/records/fda_inspections/medical-technology-products/d26d256b-7ab0-4f70-a2f8-f638a72610ee)

Company: https://www.keypedia.com/companies/medical-technology-products/51d63963-a5ce-479d-be44-afec4b0eabaa

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