# Celltrion Pharm, Inc. – FDA Inspection, Sep 14, 2023

Source: https://www.keypedia.com/records/fda_inspections/celltrion-pharm-inc/dfecf580-81e2-4327-8442-f3f986bb31c2
Source feed: FDA_Inspections

> FDA inspection 1219108 of Celltrion Pharm, Inc., September 14, 2023. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1219108
- Company Name: Celltrion Pharm, Inc.
- Inspection Date: 2023-09-14
- 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: 6

## Related Documents

- FDA Inspection 1247299 - 2024-07-23
- FDA Inspection 1209014 - 2023-06-16
- FDA Inspection 1102190 - 2019-07-12
- FDA Inspection 1034680 - 2017-11-17

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/thai-t-duong/59737092-2f30-43a7-b23b-36fa7f212c4a)

Company: https://www.keypedia.com/companies/celltrion-pharm-inc/481a4273-bf7e-4b37-8cd8-08b977ba576b

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