# The Morel Company, LLC – FDA Inspection, Nov 1, 2018

Source: https://www.keypedia.com/records/fda_inspections/the-morel-company-llc/a6be3cc6-9659-4ce8-bbab-5614334e806c
Source feed: FDA_Inspections

> FDA inspection 1070564 of The Morel Company, LLC, November 01, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation 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: 1070564
- Company Name: The Morel Company, LLC
- Inspection Date: 2018-11-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1242930 - 2024-07-02](https://www.keypedia.com/records/fda_inspections/the-morel-company-llc/96d81625-112b-4d93-82da-ec3e5ceeef3d)
- [FDA Inspection 939517 - 2015-08-27](https://www.keypedia.com/records/fda_inspections/the-morel-company-llc/5d96fe83-def3-4333-89d0-3057d8bc9a1d)

## Related Officers

- Teresa K. Kastner

Company: https://www.keypedia.com/companies/the-morel-company-llc/52396817-9113-4c3c-b344-e318e5ad2859

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