# Louis M. Gerson Co., Inc. – FDA Inspection, Jul 24, 2026

Source: https://www.keypedia.com/records/fda_inspections/louis-m-gerson-co-inc/e75646e8-fa91-4c42-be20-dac95d80882a
Source feed: FDA_Inspections

> FDA inspection 1329546 of Louis M. Gerson Co., Inc., July 24, 2026. Classification: Voluntary Action Indicated (VAI). 14 citations under 21 CFR part 803. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1329546
- Company Name: Louis M. Gerson Co., Inc.
- Inspection Date: 2026-07-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health
- Citation Count: 14

## Related Documents

- [FDA Inspection 978105 - 2016-07-26](https://www.keypedia.com/records/fda_inspections/louis-m-gerson-co-inc/2cfc1ff3-6083-4674-a6ea-cd6019dd958b)
- FDA Inspection 773444 - 2012-03-14
- FDA Inspection 556184 - 2008-11-20

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/sunita-pandey/008e5bb8-0eb3-45d8-8524-734ac0454250)

Company: https://www.keypedia.com/companies/louis-m-gerson-co-inc/a6d8c966-95df-4d5f-b36c-7aa84fb8189c

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