# Silex Medical, LLC - Inspection Records

Source: https://www.keypedia.com/companies/silex-medical-llc/218e6dd8-5da5-44d6-a66d-2b9700bb600f

> Inspection records and compliance data for Silex Medical, LLC in Southington, Connecticut. Access full analysis and detailed observations.

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## Details

- Name: Silex Medical, LLC
- FEI Number: 3005110411
- City: Southington
- State: Connecticut
- Country Name: United States
- Address Line 1: 24 Robert Porter Rd Ste B
- Zip Code: 06489

## Related Documents

- [483 - Silex Medical, LLC - 2025-04-23](https://www.keypedia.com/records/483/silex-medical-llc/e24af4c0-d58f-4b39-8fcf-24ada8d52388) — source: FDA, date: April 23, 2025
- [FDA Inspection 1268198 - Silex Medical, LLC - 2025-04-23](https://www.keypedia.com/records/fda_inspections/silex-medical-llc/720daa2c-9847-4e28-8f44-b52663809a66) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 23, 2025
- [FDA Inspection 1268198 - Silex Medical, LLC - 2025-04-23](https://www.keypedia.com/records/fda_inspections/silex-medical-llc/52c15a34-e7b1-4b3d-bae3-ad50041f9fb1) — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2025
- [FDA Inspection 1268198 - Silex Medical, LLC - 2025-04-23](https://www.keypedia.com/records/fda_inspections/silex-medical-llc/08fcda43-979d-4412-b44a-c2d8cae26a96) — classification: No Action Indicated (NAI), source: FDA, date: April 23, 2025
- [FDA Inspection 1268198 - Silex Medical, LLC - 2025-04-23](https://www.keypedia.com/records/fda_inspections/silex-medical-llc/52ff7d2f-0017-48f9-bed7-389babbdd5c5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 23, 2025
- [483 - Silex Medical, LLC - 2019-06-11](https://www.keypedia.com/records/483/silex-medical-llc/2b0faa8b-ce56-4918-b5d6-4083f3975a78) — source: FDA, date: June 11, 2019
- [FDA Inspection 1092633 - Silex Medical, LLC - 2019-06-11](https://www.keypedia.com/records/fda_inspections/silex-medical-llc/73531db1-abc2-42d4-b534-bbc8776a36f2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 11, 2019
- [FDA Inspection 1092633 - Silex Medical, LLC - 2019-06-11](https://www.keypedia.com/records/fda_inspections/silex-medical-llc/10e5cbd5-026f-4e60-bb64-3e6e827db517) — classification: No Action Indicated (NAI), source: FDA, date: June 11, 2019
- [FDA Inspection 951672 - Silex Medical, LLC - 2015-11-18](https://www.keypedia.com/records/fda_inspections/silex-medical-llc/ced743eb-c57d-4d67-897d-91896a860829) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 18, 2015
- [FDA Inspection 795339 - Silex Medical, LLC - 2012-08-22](https://www.keypedia.com/records/fda_inspections/silex-medical-llc/7889fcb8-a15b-4213-9fb3-554b4766e494) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 22, 2012

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## Related Officers

- [investigator](https://www.keypedia.com/people/michael-g-mayfield/ec045e12-d940-4f76-a17f-98ba4a8dd5b9)
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