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FDA Inspection
•ARC/Manchester, NH•April 29, 2026

ARC/Manchester, NH – FDA Inspection, Apr 29, 2026

Record Details

This FDA Inspection record concerns ARC/Manchester, NH, with an inspection on April 29, 2026, issued by the New England District Office, covering biologics.

Company
ARC/Manchester, NH
Inspection Date
April 29, 2026
Product Type
Biologics
Office
New England District Office
Person
  • Kenneth L. Smalls (Issuing Officer)
View Company Profile

ID · 244a7e90-f405-445f-b227-ef616b15aa63

Inspection Facts

Inspection number
1317006
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 640.4(f)Arm preparation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of ARC/Manchester, NH

7
DateClassificationOfficeProject area
July 28, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
February 22, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 27, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 30, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 14, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for ARC/Manchester, NH
  • FDA Inspection 1177700 - 2022-07-28
  • FDA Inspection 1045016 - 2018-02-22
  • FDA Inspection 979668 - 2016-07-27
  • FDA Inspection 878264 - 2014-04-30
  • FDA Inspection 794493 - 2012-08-14

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