FDA Inspection
Prostalund ABProstalund AB – FDA Inspection, May 31, 2019
Record Details
This FDA Inspection record concerns Prostalund AB, with an inspection on May 31, 2019, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
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ID · e1199636-2b1d-464b-b60f-0f8571b13c0f
Inspection Facts
- Inspection number
- 1092677
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 820.30(d)Design output - documentation
- 21 CFR 820.50(a)(2)Supplier oversight
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Other FDA inspections of Prostalund AB
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 17, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Prostalund AB
- FDA Inspection 580625 - 2009-04-17
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