# FDA Inspection 1329546 - Louis M. Gerson Co., Inc. - July 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 for Louis M. Gerson Co., Inc. on July 24, 2026. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1329546 - 2026-07-24](https://www.keypedia.com/records/fda_inspections/louis-m-gerson-co-inc/0c22917a-6539-436b-8ec3-96e8bcb35827)
- [FDA Inspection 978105 - 2016-07-26](https://www.keypedia.com/records/fda_inspections/louis-m-gerson-co-inc/2cfc1ff3-6083-4674-a6ea-cd6019dd958b)
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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
