FDA Inspection
Fresenius Vial SaFresenius Vial Sa – FDA Inspection, Jan 18, 2018
Record Details
This FDA Inspection record concerns Fresenius Vial Sa, with an inspection on January 18, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · d99aa1f7-5ce4-4832-8e69-834707280e6b
Inspection Facts
- Inspection number
- 1038418
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.100(b)Documentation
- 21 CFR 820.198(d)Evaluation, timeliness, identification
- 21 CFR 820.90(a)Nonconforming product control
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Other FDA inspections of Fresenius Vial Sa
1| Date | Classification | Office | Project area |
|---|---|---|---|
| January 22, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Fresenius Vial Sa
- FDA Inspection 913226 - 2015-01-22
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