# Fresenius USA Manufacturing, Inc – FDA Inspection, Oct 6, 2017

Source: https://www.keypedia.com/records/fda_inspections/fresenius-usa-manufacturing-inc/56e86173-71a4-416b-83ec-6bc5c4e27b4e
Source feed: FDA_Inspections

> FDA inspection 1028853 of Fresenius USA Manufacturing, Inc, October 06, 2017. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 211. Form 483 issued. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028853
- Company Name: Fresenius USA Manufacturing, Inc
- Inspection Date: 2017-10-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: New Drug Evaluation
- Product Type: Human Drugs
- Center: Human Drugs
- Office Name: New Orleans District Office
- Citation Count: 1

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- [FDA Inspection 1251719 - 2024-10-18](https://www.keypedia.com/records/fda_inspections/fresenius-usa-manufacturing-inc/d49f004f-328e-43b9-ac7b-3fed9a7a764a)
- FDA Inspection 1195086 - 2022-12-07
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## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brandon-c-heitmeier/09e1b64b-01de-4f8b-819a-1179d8b4c0c1)

Company: https://www.keypedia.com/companies/fresenius-usa-manufacturing-inc/6a1a5f30-4674-4964-a33e-c6401405fba9

Office: https://www.keypedia.com/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea