# FDA Inspection 1117374 - Ansh Labs, LLC - February 10, 2020

Source: https://www.keypedia.com/records/fda_inspections/ansh-labs-llc/9db8a667-564e-4933-bbf8-e12bcdbced5a
Source feed: FDA_Inspections

> FDA Inspection 1117374 for Ansh Labs, LLC on February 10, 2020. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1117374
- Company Name: Ansh Labs, LLC
- Inspection Date: 2020-02-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1117374 - 2020-02-10](https://www.keypedia.com/records/fda_inspections/ansh-labs-llc/73f04e44-f542-44cf-8e14-7cadfd09909e)

Company: https://www.keypedia.com/companies/ansh-labs-llc/b796fba8-4604-45fe-aaa7-0b37d5d211d9

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