# Remel, Inc – FDA Inspection, Jun 25, 2013

Source: https://www.keypedia.com/records/fda_inspections/remel-inc/c54b0fbe-4d6d-492d-8bba-515eb1f484a8
Source feed: FDA_Inspections

> FDA inspection 836927 of Remel, Inc, June 25, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 836927
- Company Name: Remel, Inc
- Inspection Date: 2013-06-25
- 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: 4

## Related Documents

- FDA Inspection 1199839 - 2023-03-03
- [FDA Inspection 953769 - 2015-10-23](https://www.keypedia.com/records/fda_inspections/remel-inc/cbd34b65-40d7-4b42-ba0b-9de05b2f11af)
- FDA Inspection 885210 - 2014-07-03
- FDA Inspection 823206 - 2013-03-07
- FDA Inspection 658081 - 2010-03-18

Company: https://www.keypedia.com/companies/remel-inc/f75612ef-610e-4ee4-980b-47569a492300

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