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WARNING LETTER
•Portland Sandwich Company•December 6, 2019

Portland Sandwich Company – FDA Warning Letter, Dec 6, 2019

Record Details

On April 3, 2020, the FDA issued a Warning Letter to Ms. Bracy following an inspection of her ready-to-eat (RTE) sandwich facility in Portland, Oregon, from December 2-6, 2019. The inspection revealed serious violations of the Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food regulation (21 CFR Part 117).

The FDA determined that the RTE products, including closed-face meat and cheese sandwiches, are adulterated under 21 U.S.C. § 342(a)(4) due to insanitary conditions. The facility failed to conduct a hazard analysis for any products, specifically neglecting to evaluate allergen cross-contact, undeclared allergens, environmental pathogens (e.g., Listeria, Salmonella), bacterial growth due to time/temperature control issues, and chemical hazards (e.g., mycotoxins).

The facility also failed to establish and implement preventive controls as required by 21 CFR 117.135(a)(1) and did not prepare a written food safety plan for any products, as mandated by 21 CFR 117.126(a)(1). Additionally, employees did not adhere to hygienic practices (e.g., changing tasks without discarding gloves/washing hands, bare-hand contact with food), and food manufacturing conditions did not minimize contamination

Company
Portland Sandwich Company
Inspection date
December 6, 2019
Product type
Food
Office
Division of Human and Animal Food Operations - West VI
Person
  • Miriam R. Burbach
View Company Profile

ID · 6fd9603a-7bef-4f9e-8494-bafcc7ef06fc

Violation Codes10
21 CFR 11721 U.S.C. 342(a)(4)21 U.S.C. 331(uu)21 CFR 117.130(a)21 CFR 117.130(c)(1)(ii)21 CFR 117.135(a)(1)21 CFR 117.126(a)(1)21 CFR 117.130(a)(2)21 CFR 117.135(b)21 CFR 117.139(a)

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