# Follett LLC – FDA Inspection, Oct 25, 2018

Source: https://www.keypedia.com/records/fda_inspections/follett-llc/89e46181-299b-4b2f-ae84-ff362f9ac509
Source feed: FDA_Inspections

> FDA inspection 1069935 of Follett LLC, October 25, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1069935
- Company Name: Follett LLC
- Inspection Date: 2018-10-25
- 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 1160166 - 2021-12-20](https://www.keypedia.com/records/fda_inspections/follett-llc/a9b26a68-f983-4793-9720-116dbb0ff81b)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brian-s-keefer/4fec578b-ca72-4d79-8634-3a9fe7ecd9a5)

Company: https://www.keypedia.com/companies/follett-llc/df1db2cd-64fb-43fe-9809-cc2644e8e148

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