# FDA Inspection 736645 - Lerman And Son - July 26, 2011

Source: https://www.keypedia.com/records/fda_inspections/lerman-and-son/7b56439b-f1a0-4828-8b8a-c12c45ed88c5
Source feed: FDA_Inspections

> FDA Inspection 736645 for Lerman And Son on July 26, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 736645
- Company Name: Lerman And Son
- Inspection Date: 2011-07-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/lerman-and-son/bdae5820-2d58-41c3-bc0c-fd3fc8de0b5e

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