FDA Inspection
Peter Lazic GmbhPeter Lazic Gmbh – FDA Inspection, Jul 3, 2014
Record Details
This FDA Inspection record concerns Peter Lazic Gmbh, with an inspection on July 3, 2014, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Peter Lazic Gmbh
- Inspection Date
- July 3, 2014
- Product Type
- Devices
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ID · d664dcf0-3b13-4e55-8858-25317a9a93e2
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 885943
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.75(a)Documentation
- 21 CFR 820.250(b)Sampling plans
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Other FDA inspections of Peter Lazic Gmbh
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 5, 2024 | Not classified | Office of Inspections and Investigations | Compliance: Devices |
| May 18, 2017 | Not classified | Office of Inspections and Investigations | Postmarket Assurance: Devices |
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