# Sarkli Repechage Ltd, Secaucus, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/sarkli-repechage-ltd/ff3405cd-e61e-4cbf-8d94-89ac6d8fbb25

> Inspection records and compliance data for Sarkli Repechage Ltd in Secaucus, New Jersey. 5 FDA inspections on record, last inspected November 13, 2025.

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## Details

- Name: Sarkli Repechage Ltd
- FEI Number: 3005182143
- Address Line 1: 300 Castle Rd
- City: Secaucus
- State: New Jersey
- Zip Code: 07094
- Country Name: United States
- Address: 300 Castle Rd, Secaucus, New Jersey 07094, United States
- Country: United States

## Related Documents

- FDA Inspection 1254517 - Sarkli Repechage Ltd - 2025-11-13 — source: FDA, date: November 13, 2025
- FDA Inspection 1254517 - Sarkli Repechage Ltd - 2025-11-13 — classification: No Action Indicated (NAI), source: FDA, date: November 13, 2025
- FDA Inspection 1109537 - Sarkli Repechage Ltd - 2019-09-25 — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2019
- FDA Inspection 1109537 - Sarkli Repechage Ltd - 2019-09-25 — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2019
- FDA Inspection 998401 - Sarkli Repechage Ltd - 2016-12-22 — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 22, 2016
- [FDA Inspection 975791 - Sarkli Repechage Ltd - 2016-06-22](https://www.keypedia.com/records/fda_inspections/sarkli-repechage-ltd/52e8261b-e4b5-4605-9e2a-28b5f1bec56a) — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2016
- FDA Inspection 843771 - Sarkli Repechage Ltd - 2013-08-13 — classification: No Action Indicated (NAI), source: FDA, date: August 13, 2013
- [FDA Inspection 843771 - Sarkli Repechage Ltd - 2013-08-13](https://www.keypedia.com/records/fda_inspections/sarkli-repechage-ltd/c7df5d13-db04-4dc4-8a67-e07917712154) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 13, 2013
- FDA Inspection 843771 - Sarkli Repechage Ltd - 2013-08-13 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 13, 2013

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