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FDA Inspection
•Lonza Bend Inc.•July 27, 2018

Lonza Bend Inc. – FDA Inspection, Jul 27, 2018

Record Details

This FDA Inspection record concerns Lonza Bend Inc., with an inspection on July 27, 2018, issued by the Seattle District Office, covering human drugs.

Company
Lonza Bend Inc.
Inspection Date
July 27, 2018
Product Type
Human Drugs
Office
Seattle District Office
People
  • Chiaochun J. Wang (Issuing Officer)
  • Zachary A. Bogorad
View Company Profile

ID · 73b171a0-00fd-4654-934d-25fbf8b41968

Inspection Facts

Inspection number
1060190
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Lonza Bend Inc.

7
DateClassificationOfficeProject area
May 19, 2026Not classifiedSeattle District OfficeDrug Quality Assurance
May 24, 2023VAISeattle District Office
August 5, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 27, 2018Not classifiedSeattle District Office
July 21, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Lonza Bend Inc.
  • FDA Inspection 1317820 - 2026-05-19
  • FDA Inspection 1206164 - 2023-05-24
  • FDA Inspection 1178398 - 2022-08-05
  • FDA Inspection 1065493 - 2018-07-27
  • FDA Inspection 1018924 - 2017-07-21

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