Administracion General De Servicios S.A. (ADGESA)
FDA import alert and refusal historyPueblo Libre, PeruFEI 1000375982
As of October 26, 2026, Administracion General De Servicios S.A. (ADGESA) (Pueblo Libre, Peru) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for scallops,; scallops, raw - fresh, frozen, natural state, published by FDA on September 10, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-105 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Administracion General De Servicios S.A. (ADGESA)
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 16-105red listScallops,; Scallops, Raw - Fresh, Frozen, Natural StateSource
Questions about Administracion General De Servicios S.A. (ADGESA)
- Is Administracion General De Servicios S.A. (ADGESA) on an FDA import alert?
- Yes. As of October 26, 2026, Administracion General De Servicios S.A. (ADGESA) is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for scallops,; scallops, raw - fresh, frozen, natural state; FDA published the listing on September 10, 2009.
- Has FDA refused shipments from Administracion General De Servicios S.A. (ADGESA)?
- No FDA import refusals for Administracion General De Servicios S.A. (ADGESA) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Administracion General De Servicios S.A. (ADGESA)'s FEI number?
- Administracion General De Servicios S.A. (ADGESA)'s FDA Establishment Identifier (FEI) is 1000375982.
- Can shipments from Administracion General De Servicios S.A. (ADGESA) still enter the U.S.?
- Shipments of scallops,; scallops, raw - fresh, frozen, natural state from Administracion General De Servicios S.A. (ADGESA) can be detained without physical examination under Import Alert 16-105; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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