# Janssen Cilag Manufacturing LLC – FDA Inspection, Feb 24, 2014

Source: https://www.keypedia.com/records/fda_inspections/janssen-cilag-manufacturing-llc/c1bcadc4-7acd-4f7e-a669-a42defea59ad
Source feed: FDA_Inspections

> FDA inspection 872370 of Janssen Cilag Manufacturing LLC, February 24, 2014. Classification: No Action Indicated (NAI). 9 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 872370
- Company Name: Janssen Cilag Manufacturing LLC
- Inspection Date: 2014-02-24
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1302416 - 2026-02-11](https://www.keypedia.com/records/fda_inspections/janssen-cilag-manufacturing-llc/34b6f379-9ab6-4b7e-ac2f-863b12eda16c)
- FDA Inspection 1158642 - 2021-11-23
- [FDA Inspection 1029739 - 2017-08-07](https://www.keypedia.com/records/fda_inspections/janssen-cilag-manufacturing-llc/7736c42b-93d1-4ea7-a7f5-c8f17755831d)
- FDA Inspection 998481 - 2017-01-13
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Company: https://www.keypedia.com/companies/janssen-cilag-manufacturing-llc/7d4fb569-3ecd-4de2-8235-c44b7292990f

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