# Lincotek Medical LLC. – FDA Inspection, Sep 26, 2024

Source: https://www.keypedia.com/records/fda_inspections/lincotek-medical-llc/19a7ca38-25ef-457a-a689-84a288a4deba
Source feed: FDA_Inspections

> FDA inspection 1250228 of Lincotek Medical LLC., September 26, 2024. Classification: No Action Indicated (NAI). 1 citation under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1250228
- Company Name: Lincotek Medical LLC.
- Inspection Date: 2024-09-26
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Cincinnati District Office
- Citation Count: 1

## Related Documents

- [FDA Inspection 1157207 - 2021-11-19](https://www.keypedia.com/records/fda_inspections/lincotek-medical-llc/f24f95e9-6db6-40c5-b48b-a2772efa9ae1)
- FDA Inspection 1040206 - 2018-01-12
- FDA Inspection 929478 - 2015-04-28

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/rosanna-m-goodrich/44c5c743-f67b-41fe-9cd1-8b5913bf580e)

Company: https://www.keypedia.com/companies/lincotek-medical-llc/5a3cecff-92ef-44e0-ab46-8c4d150b0d95

Office: https://www.keypedia.com/offices/cincinnati-district-office/b67a0c35-82e3-4176-9039-988378f65c22