# GP Pharm SA – FDA Inspection, Jan 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/gp-pharm-sa/d67f0658-9a83-4622-a757-b6a1542990ad
Source feed: FDA_Inspections

> FDA inspection 1004446 of GP Pharm SA, January 24, 2017. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 211 and 820. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1004446
- Company Name: GP Pharm SA
- Inspection Date: 2017-01-24
- 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: 7

## Related Documents

- FDA Inspection 1305252 - 2023-09-21
- FDA Inspection 1149441 - 2020-10-02
- [FDA Inspection 1091594 - 2019-05-21](https://www.keypedia.com/records/fda_inspections/gp-pharm-sa/9007b864-97a5-4e91-b3db-d9515b083a72)
- FDA Inspection 1062872 - 2018-06-20
- FDA Inspection 917365 - 2015-01-27

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/katherine-e-jacobitz/9a713b44-95c4-43a2-83bb-8d30062d8345)
- [FDA Associated Person](https://www.keypedia.com/people/uttaniti-limchumroon/ce890cbf-2f5c-498f-917c-0edf8b10d356)

Company: https://www.keypedia.com/companies/gp-pharm-sa/dc9c0e23-15fc-4984-99e1-68b6e5ad0899

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