# Clareblend, Inc. – FDA Inspection, Jul 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/clareblend-inc/674fd91e-022e-415d-a48d-0e07b404fc72
Source feed: FDA_Inspections

> FDA inspection 937413 of Clareblend, Inc., July 17, 2015. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- [FDA Inspection 1055147 - 2018-06-08](https://www.keypedia.com/records/fda_inspections/clareblend-inc/a2324f9f-8f09-460d-b093-8384dce06a74)
- FDA Inspection 806360 - 2012-11-14

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

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