# Stihler Electronic Gmbh – FDA Inspection, Dec 6, 2018

Source: https://www.keypedia.com/records/fda_inspections/stihler-electronic-gmbh/4568957a-f882-4886-91f2-edcbbe436772
Source feed: FDA_Inspections

> FDA inspection 1073764 of Stihler Electronic Gmbh, December 06, 2018. 2 citations under 21 CFR parts 803 and 806. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073764
- Company Name: Stihler Electronic Gmbh
- Inspection Date: 2018-12-06
- Project Area: Postmarket Assurance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 2

## Related Documents

- FDA Inspection 902860 - 2014-10-27
- FDA Inspection 631160 - 2009-11-09

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

Company: https://www.keypedia.com/companies/stihler-electronic-gmbh/3cb2d870-bc16-4a08-b78d-5d78b2951d71

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8