FDA Inspection
Raumedic AG Werk ZwoenitzRaumedic AG Werk Zwoenitz – FDA Inspection, Jan 29, 2015
Record Details
This FDA Inspection record concerns Raumedic AG Werk Zwoenitz, with an inspection on January 29, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Raumedic AG Werk Zwoenitz
- Inspection Date
- January 29, 2015
- Product Type
- Devices
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ID · 0e9e01eb-1b13-4e51-8047-5aeb91ce90cf
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 917699
- 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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