# Clareblend, Inc. – FDA Inspection, Jun 8, 2018

Source: https://www.keypedia.com/records/fda_inspections/clareblend-inc/a2324f9f-8f09-460d-b093-8384dce06a74
Source feed: FDA_Inspections

> FDA inspection 1055147 of Clareblend, Inc., June 08, 2018. Classification: No Action Indicated (NAI). 11 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1055147
- Company Name: Clareblend, Inc.
- Inspection Date: 2018-06-08
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 11

## Related Documents

- [FDA Inspection 937413 - 2015-07-17](https://www.keypedia.com/records/fda_inspections/clareblend-inc/674fd91e-022e-415d-a48d-0e07b404fc72)
- FDA Inspection 806360 - 2012-11-14

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/james-r-montero/ce2d19fd-25b7-423e-9132-5d6f582380d2)

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