# Intersurgical Inc, East Syracuse, NY – FDA Inspections

Source: https://www.keypedia.com/companies/intersurgical-inc/7056e323-cd0a-435a-8cd8-694f6ae6c4bc

> Inspection records and compliance data for Intersurgical Inc in East Syracuse, New York. 5 FDA inspections on record, 1 Form 483, last inspected September 11, 2024.

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## Details

- Name: Intersurgical Inc
- FEI Number: 1000120301
- Address Line 1: 5010 Campuswood Dr Ste 102
- City: East Syracuse
- State: New York
- Zip Code: 13057
- Country Name: United States
- Address: 5010 Campuswood Dr Ste 102, East Syracuse, New York 13057, United States
- Country: United States

## Related Documents

- FDA Inspection 1249149 - Intersurgical Inc - 2024-09-11 — source: FDA, date: September 11, 2024
- FDA Inspection 1249149 - Intersurgical Inc - 2024-09-11 — classification: No Action Indicated (NAI), source: FDA, date: September 11, 2024
- FDA Inspection 1249149 - Intersurgical Inc - 2024-09-11 — classification: No Action Indicated (NAI), source: FDA, date: September 11, 2024
- FDA Inspection 1071317 - Intersurgical Inc - 2018-11-01 — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2018
- FDA Inspection 1071317 - Intersurgical Inc - 2018-11-01 — classification: No Action Indicated (NAI), source: FDA, date: November 1, 2018
- FDA Inspection 993336 - Intersurgical Inc - 2016-11-18 — classification: No Action Indicated (NAI), source: FDA, date: November 18, 2016
- [FDA Inspection 993336 - Intersurgical Inc - 2016-11-18](https://www.keypedia.com/records/fda_inspections/intersurgical-inc/9e4bc443-22e4-4a6d-9efb-94b380bcbaad) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 18, 2016
- FDA Inspection 903122 - Intersurgical Inc - 2014-10-29 — classification: No Action Indicated (NAI), source: FDA, date: October 29, 2014
- FDA Inspection 903122 - Intersurgical Inc - 2014-10-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 29, 2014
- FDA Inspection 760050 - Intersurgical Inc - 2011-12-21 — classification: No Action Indicated (NAI), source: FDA, date: December 21, 2011

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