# Lowell, Inc. – FDA Inspection, Mar 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/lowell-inc/ff2c81fb-9a51-4e1b-b44f-b2bf32fc1daa
Source feed: FDA_Inspections

> FDA inspection 1004052 of Lowell, Inc., March 10, 2017. 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: 1004052
- Company Name: Lowell, Inc.
- Inspection Date: 2017-03-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1194244 - 2022-12-06](https://www.keypedia.com/records/fda_inspections/lowell-inc/df02af65-7d6d-47db-890d-9ad5e08e8091)
- FDA Inspection 729519 - 2011-06-08

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/benjamin-w-anderson/a3c0961c-6a83-4bd7-abb8-02c5c8dd3a35)

Company: https://www.keypedia.com/companies/lowell-inc/c3435694-b207-45cf-90bf-845a2ab54843

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