FDA Inspection
Weba Medizintechnik GmbH & Co.Weba Medizintechnik GmbH & Co. – FDA Inspection, Mar 11, 2015
Record Details
This FDA Inspection record concerns Weba Medizintechnik GmbH & Co., with an inspection on March 11, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- March 11, 2015
- Product Type
- Devices
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ID · de7536eb-d517-47d7-8635-6855e8225a37
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 919425
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 803.50(a)(2)Individual Report of Malfunction
- 21 CFR 820.72(a)Equipment suitability & capability
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