# Lincotek Medical LLC., Vandalia, OH – FDA Inspections

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

> Inspection records and compliance data for Lincotek Medical LLC. in Vandalia, Ohio. 4 FDA inspections on record, 1 Form 483, last inspected September 26, 2024.

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## Details

- Name: Lincotek Medical LLC.
- FEI Number: 3010039400
- Address Line 1: 811 Northwoods Blvd
- City: Vandalia
- State: Ohio
- Zip Code: 45377
- Country Name: United States
- Address: 811 Northwoods Blvd, Vandalia, Ohio 45377, United States
- Country: United States

## Related Documents

- FDA Inspection 1250228 - Lincotek Medical LLC. - 2024-09-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 26, 2024
- [FDA Inspection 1250228 - Lincotek Medical LLC. - 2024-09-26](https://www.keypedia.com/records/fda_inspections/lincotek-medical-llc/19a7ca38-25ef-457a-a689-84a288a4deba) — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2024
- FDA Inspection 1250228 - Lincotek Medical LLC. - 2024-09-26 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 26, 2024
- FDA Inspection 1250228 - Lincotek Medical LLC. - 2024-09-26 — classification: No Action Indicated (NAI), source: FDA, date: September 26, 2024
- [FDA Inspection 1157207 - Lincotek Medical LLC. - 2021-11-19](https://www.keypedia.com/records/fda_inspections/lincotek-medical-llc/f24f95e9-6db6-40c5-b48b-a2772efa9ae1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 19, 2021
- FDA Inspection 1157207 - Lincotek Medical LLC. - 2021-11-19 — classification: No Action Indicated (NAI), source: FDA, date: November 19, 2021
- FDA Inspection 1040206 - Lincotek Medical LLC. - 2018-01-12 — classification: No Action Indicated (NAI), source: FDA, date: January 12, 2018
- FDA Inspection 1040206 - Lincotek Medical LLC. - 2018-01-12 — classification: No Action Indicated (NAI), source: FDA, date: January 12, 2018
- FDA Inspection 929478 - Lincotek Medical LLC. - 2015-04-28 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 28, 2015

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