# FDA Inspection 937413 - Clareblend, Inc. - July 17, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/clareblend-inc/278458a6-d602-4c47-8691-e52394ab9fcc
Source feed: FDA_Inspections

> FDA Inspection 937413 for Clareblend, Inc. on July 17, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 937413
- Company Name: Clareblend, Inc.
- Inspection Date: 2015-07-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1055147 - 2018-06-08](https://www.globalkeysolutions.net/records/fda_inspections/clareblend-inc/38f337d1-c2e7-4447-8e76-b7e249ad8f04)
- [FDA Inspection 1055147 - 2018-06-08](https://www.globalkeysolutions.net/records/fda_inspections/clareblend-inc/a2324f9f-8f09-460d-b093-8384dce06a74)
- [FDA Inspection 937413 - 2015-07-17](https://www.globalkeysolutions.net/records/fda_inspections/clareblend-inc/674fd91e-022e-415d-a48d-0e07b404fc72)
- [FDA Inspection 806360 - 2012-11-14](https://www.globalkeysolutions.net/records/fda_inspections/clareblend-inc/ab0074f0-fd5c-4601-9c0d-55bf3641b599)
- [FDA Inspection 806360 - 2012-11-14](https://www.globalkeysolutions.net/records/fda_inspections/clareblend-inc/1ad147cb-3431-49cf-a31f-6f0fade37f20)

Company: https://www.globalkeysolutions.net/companies/clareblend-inc/2863e06d-2a07-49ca-bc2e-8ab2ce80e665

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