# FDA Inspection 1010935 - Impulse Dynamics (USA), Inc. - May 18, 2017

Source: https://www.keypedia.com/records/fda_inspections/impulse-dynamics-usa-inc/66b3932a-e3a9-4b40-bf3f-31f6116ee21d
Source feed: FDA_Inspections

> FDA Inspection 1010935 for Impulse Dynamics (USA), Inc. on May 18, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010935
- Company Name: Impulse Dynamics (USA), Inc.
- Inspection Date: 2017-05-18
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 772328 - 2012-02-24](https://www.keypedia.com/records/fda_inspections/impulse-dynamics-usa-inc/01715fde-7462-4dfa-a59a-996da478466c)

Company: https://www.keypedia.com/companies/impulse-dynamics-usa-inc/db53003f-19fa-48f0-97b3-351b61491e06

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