# Bio-Med Devices, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/bio-med-devices-inc/39493c09-314b-444a-9c89-2dae1ee10bc9

> Inspection records and compliance data for Bio-Med Devices, Inc. in Guilford, Connecticut. Access full analysis and detailed observations.

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## Details

- Name: Bio-Med Devices, Inc.
- FEI Number: 3003952420
- City: Guilford
- State: Connecticut
- Country Name: United States
- Address Line 1: 61 Soundview Rd
- Zip Code: 06437

## Related Documents

- [FDA Inspection 1257848 - Bio-Med Devices, Inc. - 2024-12-20](https://www.keypedia.com/records/fda_inspections/bio-med-devices-inc/880fe2bc-14d0-47b4-93d4-272492b115c9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 20, 2024
- [FDA Inspection 1257848 - Bio-Med Devices, Inc. - 2024-12-20](https://www.keypedia.com/records/fda_inspections/bio-med-devices-inc/dfa604c1-b832-4117-b047-12438d1e16fc) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2024
- [FDA Inspection 1257848 - Bio-Med Devices, Inc. - 2024-12-20](https://www.keypedia.com/records/fda_inspections/bio-med-devices-inc/798e9d29-5e56-4e0a-b0bb-2a5ed543f420) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 20, 2024
- [FDA Inspection 1257848 - Bio-Med Devices, Inc. - 2024-12-20](https://www.keypedia.com/records/fda_inspections/bio-med-devices-inc/a02e68b5-8a1e-4da7-a444-090f3764ffbd) — classification: No Action Indicated (NAI), source: FDA, date: December 20, 2024
- [483 - Bio-Med Devices, Inc. - 2022-03-31](https://www.keypedia.com/records/483/bio-med-devices-inc/93914fe9-3e97-49f6-bf5e-6fb2858ff28f) — source: FDA, date: March 31, 2022
- [FDA Inspection 1166532 - Bio-Med Devices, Inc. - 2022-03-31](https://www.keypedia.com/records/fda_inspections/bio-med-devices-inc/58553afe-a67d-4cf5-b021-7f32082c264b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2022
- [FDA Inspection 1166532 - Bio-Med Devices, Inc. - 2022-03-31](https://www.keypedia.com/records/fda_inspections/bio-med-devices-inc/880301da-2bc0-414f-b59d-ab74fece6ecd) — classification: No Action Indicated (NAI), source: FDA, date: March 31, 2022
- [FDA Inspection 980898 - Bio-Med Devices, Inc. - 2016-08-18](https://www.keypedia.com/records/fda_inspections/bio-med-devices-inc/b3ceb2e0-a236-484c-89ae-aa4e301f13d8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 18, 2016
- [FDA Inspection 980898 - Bio-Med Devices, Inc. - 2016-08-18](https://www.keypedia.com/records/fda_inspections/bio-med-devices-inc/67ac6f0d-c103-4870-9f55-293c249963f0) — classification: No Action Indicated (NAI), source: FDA, date: August 18, 2016
- [FDA Inspection 727724 - Bio-Med Devices, Inc. - 2011-05-26](https://www.keypedia.com/records/fda_inspections/bio-med-devices-inc/eaf7e102-d699-41e6-8883-2cdb2cf7bf65) — classification: No Action Indicated (NAI), source: FDA, date: May 26, 2011

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