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Canberra Corporation

FEI 1000508133 · 3610 N Holland Sylvania Rd, Toledo, Ohio, 43615, United States

Per FDA, as of 2026-10-31 · Sources: FDA Data Dashboard, Import Alerts, Enforcement Reports

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Import alerts
0
Import refusals (5 years)
0
Warning letters
0
Last FDA action
2013-02-21
13 years ago

FDA record

  1. 2013-02-21
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Colors and Cosmetics Technology
    FDA source
  2. 2010-09-14
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Colors and Cosmetics Technology
    FDA source
  3. 2010-08-11
    InspectionFDA inspection · Classification: Voluntary Action Indicated (VAI)
    Project area: Colors and Cosmetics Technology
    FDA source
  4. 2010-06-07
    RecallRecall F-2650-2010 · Class 2 · The firm received a complaint from a customer indicating that the product may be contaminated with Pseudomonas putida. The firm tested retain samples of the product and the results was positive for gram negative Pseudomonas aeruginosa.
    Osceola Perineal Solution with Aloe Vera 8 fl. oz. bottle. Lot # 45-11239C
    Source: FDA Enforcement Reports