# Recipharm HC Limited - Inspection Records

Source: https://www.globalkeysolutions.net/companies/recipharm-hc-limited/8a43ba03-736e-449b-8f0e-ce56d8655d56

> Inspection records and compliance data for Recipharm HC Limited in Crewe, None. Access full analysis and detailed observations.

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## Details

- Name: Recipharm HC Limited
- FEI Number: 3001621739
- City: Crewe
- State: None
- Country Name: United Kingdom
- Address Line 1: London Road
- Zip Code: None

## Related Documents

- [FDA Inspection 1156170 - Recipharm HC Limited - 2020-11-26](https://www.globalkeysolutions.net/records/fda_inspections/recipharm-hc-limited/d41abd61-dd46-45af-a3b5-218694015455) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 26, 2020
- [FDA Inspection 1065951 - Recipharm HC Limited - 2017-11-10](https://www.globalkeysolutions.net/records/fda_inspections/recipharm-hc-limited/dcdcf462-92d0-4446-a89a-b911a47e1691) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 10, 2017
- [FDA Inspection 956577 - Recipharm HC Limited - 2016-01-15](https://www.globalkeysolutions.net/records/fda_inspections/recipharm-hc-limited/061059ec-a3a8-458b-b687-d3702d6234b1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 15, 2016
- [FDA Inspection 869740 - Recipharm HC Limited - 2014-03-07](https://www.globalkeysolutions.net/records/fda_inspections/recipharm-hc-limited/552bdd00-7474-4efb-a7ac-d08da741dcfe) — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2014
- [FDA Inspection 748166 - Recipharm HC Limited - 2011-09-09](https://www.globalkeysolutions.net/records/fda_inspections/recipharm-hc-limited/98ddc742-cdfb-4915-a179-522c40a887fd) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 9, 2011
- [FDA Inspection 618011 - Recipharm HC Limited - 2009-08-28](https://www.globalkeysolutions.net/records/fda_inspections/recipharm-hc-limited/6166cf15-af1d-4514-8332-831d462c4de3) — classification: No Action Indicated (NAI), source: FDA, date: August 28, 2009

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