# Buckhead Meat & Seafood Mid Atlantic, Inc., Landover, MD – FDA Inspections

Source: https://www.keypedia.com/companies/buckhead-meat-seafood-mid-atlantic-inc/82aa8db2-4bd7-409e-ac2f-6acf514c2605

> Inspection records and compliance data for Buckhead Meat & Seafood Mid Atlantic, Inc. in Landover, Maryland. 8 FDA inspections on record, 1 Form 483, last inspected January 08, 2026.

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## Details

- Name: Buckhead Meat & Seafood Mid Atlantic, Inc.
- FEI Number: 3000717770
- Address Line 1: 1920 Stanford Ct
- City: Landover
- State: Maryland
- Zip Code: 20785
- Country Name: United States
- Address: 1920 Stanford Ct, Landover, Maryland 20785, United States
- Country: United States

## Related Documents

- [FDA Inspection 1285215 - Buckhead Meat & Seafood Mid Atlantic, Inc. - 2026-01-08](https://www.keypedia.com/records/fda_inspections/buckhead-meat-seafood-mid-atlantic-inc/32984c39-80c6-462d-99cc-d5256e2fa613) — source: FDA, date: January 8, 2026
- FDA Inspection 1210831 - Buckhead Meat & Seafood Mid Atlantic, Inc. - 2023-07-17 — source: FDA, date: July 17, 2023
- FDA Inspection 1100627 - Buckhead Meat & Seafood Mid Atlantic, Inc. - 2019-08-26 — source: FDA, date: August 26, 2019
- [FDA Inspection 997253 - Buckhead Meat & Seafood Mid Atlantic, Inc. - 2017-01-09](https://www.keypedia.com/records/fda_inspections/buckhead-meat-seafood-mid-atlantic-inc/f306d6e6-315e-4794-97e3-67f2832bd03a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 9, 2017
- FDA Inspection 831778 - Buckhead Meat & Seafood Mid Atlantic, Inc. - 2013-05-15 — classification: No Action Indicated (NAI), source: FDA, date: May 15, 2013
- FDA Inspection 814232 - Buckhead Meat & Seafood Mid Atlantic, Inc. - 2013-01-09 — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2013
- FDA Inspection 662111 - Buckhead Meat & Seafood Mid Atlantic, Inc. - 2010-04-09 — classification: No Action Indicated (NAI), source: FDA, date: April 9, 2010
- FDA Inspection 631604 - Buckhead Meat & Seafood Mid Atlantic, Inc. - 2009-12-01 — classification: No Action Indicated (NAI), source: FDA, date: December 1, 2009

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