FDA Inspection
Sanmina Ireland Unlimited CompanySanmina Ireland Unlimited Company – FDA Inspection, Sep 14, 2023
Record Details
This FDA Inspection record concerns Sanmina Ireland Unlimited Company, with an inspection on September 14, 2023, issued by the Center for Devices and Radiological Health, covering devices.
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ID · e5aa10c1-8776-4e46-acd0-fbd491208fb9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1217651
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
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Other FDA inspections of Sanmina Ireland Unlimited Company
2| Date | Classification | Office | Project area |
|---|---|---|---|
| May 28, 2026 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
| September 25, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Sanmina Ireland Unlimited Company
- FDA Inspection 1319324 - 2026-05-28
- FDA Inspection 900361 - 2014-09-25
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