# Tri-State Surgical Supply & Equipment LTD - Inspection Records

Source: https://www.globalkeysolutions.net/companies/tri-state-surgical-supply-equipment-ltd/c4ef7a1b-cb20-46cd-9a4d-701e27b2332d

> Inspection records and compliance data for Tri-State Surgical Supply & Equipment LTD in Brooklyn, New York. Access full analysis and detailed observations.

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## Details

- Name: Tri-State Surgical Supply & Equipment LTD
- FEI Number: 2433559
- City: Brooklyn
- State: New York
- Country Name: United States
- Address Line 1: 409 Hoyt St
- Zip Code: 11231

## Related Documents

- [FDA Inspection 942093 - Tri-State Surgical Supply & Equipment LTD - 2015-09-10](https://www.globalkeysolutions.net/records/fda_inspections/tri-state-surgical-supply-equipment-ltd/0658b3d2-f1fa-4e13-8afa-4aa0021793a7) — classification: No Action Indicated (NAI), source: FDA, date: September 10, 2015
- [FDA Inspection 798942 - Tri-State Surgical Supply & Equipment LTD - 2012-09-13](https://www.globalkeysolutions.net/records/fda_inspections/tri-state-surgical-supply-equipment-ltd/7796ab13-bcbd-4003-a583-354bfd7477ec) — classification: No Action Indicated (NAI), source: FDA, date: September 13, 2012
- [FDA Inspection 704629 - Tri-State Surgical Supply & Equipment LTD - 2011-01-05](https://www.globalkeysolutions.net/records/fda_inspections/tri-state-surgical-supply-equipment-ltd/ee86ce88-2c26-4252-a0ba-eff63ff343f4) — classification: No Action Indicated (NAI), source: FDA, date: January 5, 2011
- [FDA Inspection 644968 - Tri-State Surgical Supply & Equipment LTD - 2010-02-09](https://www.globalkeysolutions.net/records/fda_inspections/tri-state-surgical-supply-equipment-ltd/35452111-7709-4a0b-ba66-ffbede73de7f) — classification: No Action Indicated (NAI), source: FDA, date: February 9, 2010
- [FDA Inspection 603229 - Tri-State Surgical Supply & Equipment LTD - 2009-08-07](https://www.globalkeysolutions.net/records/fda_inspections/tri-state-surgical-supply-equipment-ltd/c359850c-a114-4e3e-b57d-f1bc4687438a) — classification: No Action Indicated (NAI), source: FDA, date: August 7, 2009

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