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If a private laboratory is used, further information regarding private laboratory analyses is found in FDA's ORA Lab Manual, volume III, section 7. Such evidence should be submitted to the appropriate FDA Division Compliance Office for consideration, per the notice of detention. Such evidence may include private laboratory analysis of samples.

All requests for addition to DWPE will be evaluated by the Division of Import Operations (DIO) and when necessary will consult with the Center for Food Safety and Applied Nutrition (CFSAN), Office of Compliance, Division of Enforcement.*** Release of Articles Subject to Detention Without Physical Examination under This Import Alert: ***In order to secure release of an individual shipment identified for DWPE under this import alert, the owner, consignee and/or another responsible party to the shipment should provide evidence which demonstrates that the product does not bear or contain pesticide chemical residues that are unsafe within the meaning of section 408(a) of the Federal Food, Drug & Cosmetic Act (21 U.S.C.

In accordance with Chapter 9 of the Regulatory Procedures Manual, recommendations for addition to detention without physical examination for raw agricultural commodity product(s) from an individual firm may be made after one violative entry if it contains actionable levels of a pesticide chemical residue and all other appropriate criteria are satisfied.

*** Divisions may detain, without physical examination, shipments of specified products from firms identified on the Red List of this Import Alert.

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