# Ward Cove Dock Group LLC - M/V Malaspina, Ketchikan, AK – FDA Inspections

Source: https://www.keypedia.com/companies/ward-cove-dock-group-llc-mv-malaspina/a7e7f777-919e-4d1c-b0b3-97cd59087c71

> Inspection records and compliance data for Ward Cove Dock Group LLC - M/V Malaspina in Ketchikan, Alaska. 8 FDA inspections on record, 1 Form 483, last inspected March 17, 2017.

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## Details

- Name: Ward Cove Dock Group LLC - M/V Malaspina
- FEI Number: 3004717152
- Address Line 1: Ward Cove
- City: Ketchikan
- State: Alaska
- Zip Code: 99901
- Country Name: United States
- Address: Ward Cove, Ketchikan, Alaska 99901, United States
- Country: United States

## Related Documents

- [FDA Inspection 1009440 - Ward Cove Dock Group LLC - M/V Malaspina - 2017-03-17](https://www.keypedia.com/records/fda_inspections/ward-cove-dock-group-llc-mv-malaspina/a11e6e5a-be16-4133-ab9a-371d2f7fe1c3) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 17, 2017
- FDA Inspection 922440 - Ward Cove Dock Group LLC - M/V Malaspina - 2015-04-10 — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2015
- FDA Inspection 918994 - Ward Cove Dock Group LLC - M/V Malaspina - 2015-03-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 20, 2015
- FDA Inspection 870092 - Ward Cove Dock Group LLC - M/V Malaspina - 2014-02-21 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 21, 2014
- FDA Inspection 722198 - Ward Cove Dock Group LLC - M/V Malaspina - 2011-03-04 — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2011
- FDA Inspection 657386 - Ward Cove Dock Group LLC - M/V Malaspina - 2010-03-19 — classification: No Action Indicated (NAI), source: FDA, date: March 19, 2010
- FDA Inspection 649801 - Ward Cove Dock Group LLC - M/V Malaspina - 2010-02-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 5, 2010
- FDA Inspection 584382 - Ward Cove Dock Group LLC - M/V Malaspina - 2009-01-23 — classification: No Action Indicated (NAI), source: FDA, date: January 23, 2009

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