FDA Inspection
Novo Nordisk A/SNovo Nordisk A/S – FDA Inspection, Mar 21, 2013
Record Details
This FDA Inspection record concerns Novo Nordisk A/S, with an inspection on March 21, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Novo Nordisk A/S
- Inspection Date
- March 21, 2013
- Product Type
- Devices
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ID · 7a092c06-c647-4cd1-85c9-e6676765c20f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 830061
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
1- 21 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate
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