FDA Inspection
Stihler Electronic GmbhStihler Electronic Gmbh – FDA Inspection, Dec 6, 2018
Record Details
This FDA Inspection record concerns Stihler Electronic Gmbh, with an inspection on December 6, 2018, issued by the Office of Inspections and Investigations, covering medical devices & rad health.
- Company
- Stihler Electronic Gmbh
- Inspection Date
- December 6, 2018
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · 4568957a-f882-4886-91f2-edcbbe436772
Inspection Facts
- Inspection number
- 1073764
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 803.50(b)(2)Providing Incomplete or Missing Information
- 21 CFR 806.10(a)(1)Report of risk to health
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Other FDA inspections of Stihler Electronic Gmbh
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 27, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 9, 2009 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Stihler Electronic Gmbh
- FDA Inspection 902860 - 2014-10-27
- FDA Inspection 631160 - 2009-11-09
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