# Roper's Fish House, Myrtle Beach, SC – FDA Inspections

Source: https://www.keypedia.com/companies/ropers-fish-house/c92d7b7d-12ba-4109-8da3-b30b76b71f29

> Inspection records and compliance data for Roper's Fish House in Myrtle Beach, South Carolina. 5 FDA inspections on record, 1 Form 483, last inspected August 14, 2017.

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## Details

- Name: Roper's Fish House
- FEI Number: 3004067286
- Address Line 1: 4655 Socastee Blvd Bldg A
- City: Myrtle Beach
- State: South Carolina
- Zip Code: 29588
- Country Name: United States
- Address: 4655 Socastee Blvd Bldg A, Myrtle Beach, South Carolina 29588, United States
- Country: United States

## Related Documents

- [FDA Inspection 1021630 - Roper's Fish House - 2017-08-14](https://www.keypedia.com/records/fda_inspections/ropers-fish-house/92e93639-4108-4d81-8a0b-40f347875d41) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 14, 2017
- [FDA Inspection 889882 - Roper's Fish House - 2014-07-31](https://www.keypedia.com/records/fda_inspections/ropers-fish-house/e8ffe1fc-1fa2-4c83-b112-c47f6015e3f5) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 31, 2014
- [FDA Inspection 701826 - Roper's Fish House - 2010-12-03](https://www.keypedia.com/records/fda_inspections/ropers-fish-house/8738cb99-bb27-4bb1-8e2b-f503152f130b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 3, 2010
- FDA Inspection 630961 - Roper's Fish House - 2009-11-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 20, 2009
- FDA Inspection 630961 - Roper's Fish House - 2009-11-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 20, 2009
- FDA Inspection 593442 - Roper's Fish House - 2009-04-24 — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2009
- FDA Inspection 593442 - Roper's Fish House - 2009-04-24 — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 24, 2009
- FDA Inspection 593442 - Roper's Fish House - 2009-04-24 — classification: No Action Indicated (NAI), source: FDA, date: April 24, 2009

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