# LifeCell Corporation – FDA Inspection, Jun 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/lifecell-corporation/be72417e-72ae-4bfd-b0f0-d068e8c12541
Source feed: FDA_Inspections

> FDA inspection 1095091 of LifeCell Corporation, June 14, 2019. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 12 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1095091
- Company Name: LifeCell Corporation
- Inspection Date: 2019-06-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1329332 - 2026-09-21](https://www.keypedia.com/records/fda_inspections/lifecell-corporation/88f4f8d7-7d1a-4e6e-b3c2-96d19d3301db)
- FDA Inspection 1230349 - 2024-05-21
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- [FDA Inspection 1089602 - 2019-01-10](https://www.keypedia.com/records/fda_inspections/lifecell-corporation/fb559597-19ce-42e5-86ae-79a0ab93f936)
- FDA Inspection 1028651 - 2017-09-27

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/frank-j-marciniak/6995351a-6afc-4056-9692-d4aeb711dd92)

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

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