# FDA Inspection 711502 - Johnson & Johnson Products - January 20, 2011

Source: https://www.keypedia.com/records/fda_inspections/johnson-johnson-products/9d747ebb-1e56-4e11-ad53-b0f856d95617
Source feed: FDA_Inspections

> FDA Inspection 711502 for Johnson & Johnson Products on January 20, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 711502
- Company Name: Johnson & Johnson Products
- Inspection Date: 2011-01-20
- 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/johnson-johnson-products/0b18816a-d47f-4d61-ae33-8e1ed23c43a2

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