FDA Inspection
Arcoma ABArcoma AB – FDA Inspection, Jan 19, 2010
Record Details
This FDA Inspection record concerns Arcoma AB, with an inspection on January 19, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Arcoma AB
- Inspection Date
- January 19, 2010
- Product Type
- Devices
View Company Profile
ID · 036502eb-ce5e-4825-9730-48fbd2a19310
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 646909
- FDA center
- Medical Devices & Rad Health
- Project area
- Radiation Control and Health Safety Act
FDA Citations
1- 21 CFR 1020.30(n)Compliance measurement
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Arcoma AB
1| Date | Classification | Office | Project area |
|---|---|---|---|
| June 27, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Arcoma AB
- FDA Inspection 839779 - 2013-06-27
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