# Rog Sports Medicine Inc, Orland Park, IL – FDA Inspections

Source: https://www.keypedia.com/companies/rog-sports-medicine-inc/36b967c4-c556-4f4e-b641-ae8ad56b51ea

> Inspection records and compliance data for Rog Sports Medicine Inc in Orland Park, Illinois. 4 FDA inspections on record, last inspected November 12, 2024.

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## Details

- Name: Rog Sports Medicine Inc
- FEI Number: 3009227834
- Address Line 1: 16450 104th Ave
- City: Orland Park
- State: Illinois
- Zip Code: 60467
- Country Name: United States
- Address: 16450 104th Ave, Orland Park, Illinois 60467, United States
- Country: United States

## Related Documents

- FDA Inspection 1254978 - Rog Sports Medicine Inc - 2024-11-12 — source: FDA, date: November 12, 2024
- [FDA Inspection 1254978 - Rog Sports Medicine Inc - 2024-11-12](https://www.keypedia.com/records/fda_inspections/rog-sports-medicine-inc/c578fb60-fa41-4245-bcc5-daecd49970f5) — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2024
- FDA Inspection 1254978 - Rog Sports Medicine Inc - 2024-11-12 — classification: No Action Indicated (NAI), source: FDA, date: November 12, 2024
- [FDA Inspection 1153903 - Rog Sports Medicine Inc - 2021-09-29](https://www.keypedia.com/records/fda_inspections/rog-sports-medicine-inc/8d94a34d-139d-4221-9dcd-1976d97688bd) — classification: No Action Indicated (NAI), source: FDA, date: September 29, 2021
- FDA Inspection 1153903 - Rog Sports Medicine Inc - 2021-09-29 — classification: No Action Indicated (NAI), source: FDA, date: September 29, 2021
- FDA Inspection 915942 - Rog Sports Medicine Inc - 2015-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2015
- FDA Inspection 915942 - Rog Sports Medicine Inc - 2015-02-12 — classification: No Action Indicated (NAI), source: FDA, date: February 12, 2015
- FDA Inspection 808511 - Rog Sports Medicine Inc - 2012-10-31 — classification: No Action Indicated (NAI), source: FDA, date: October 31, 2012
- FDA Inspection 808511 - Rog Sports Medicine Inc - 2012-10-31 — classification: No Action Indicated (NAI), source: FDA, date: October 31, 2012

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