# FDA Inspection 980020 - LifeCell Corporation - June 21, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/lifecell-corporation/ff99eb61-216d-410f-915d-62a366718b9b/
Source feed: FDA_Inspections

> FDA Inspection 980020 for LifeCell Corporation on June 21, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980020
- Company Name: LifeCell Corporation
- Inspection Date: 2016-06-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/lifecell-corporation/befaec51-e133-4222-ad7e-0cf8e59f5d23

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