# FDA Inspection 978105 - Louis M. Gerson Co., Inc. - July 26, 2016

Source: https://www.keypedia.com/records/fda_inspections/louis-m-gerson-co-inc/2cfc1ff3-6083-4674-a6ea-cd6019dd958b
Source feed: FDA_Inspections

> FDA Inspection 978105 for Louis M. Gerson Co., Inc. on July 26, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 978105
- Company Name: Louis M. Gerson Co., Inc.
- Inspection Date: 2016-07-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 773444 - 2012-03-14](https://www.keypedia.com/records/fda_inspections/louis-m-gerson-co-inc/3120dc29-8975-497f-82a9-25735f5e6376)
- [FDA Inspection 556184 - 2008-11-20](https://www.keypedia.com/records/fda_inspections/louis-m-gerson-co-inc/6f8ba011-da73-4f74-b675-835029464504)

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
