FDA Inspection
ABS CorporationABS Corporation – FDA Inspection, Feb 27, 2017
Record Details
This FDA Inspection record concerns ABS Corporation, with an inspection on February 27, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · d7f376f5-7603-47d8-8103-8fe2e5e56059
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1002791
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 211.192Quality control unit review of records
- 21 CFR 211.192Written record of investigation incomplete
- 21 CFR 211.198(a)Procedures to be written and followed
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
- 21 CFR 820.40(b)Document change records, maintained.
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Other FDA inspections of ABS Corporation
10| Date | Classification | Office | Project area |
|---|---|---|---|
| January 16, 2026 | Not classified | Kansas City District Office | Monitoring of Marketed Animal Drugs, Feeds, and Devices |
| April 29, 2025 | Not classified | Kansas City District Office | |
| August 13, 2024 | NAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
| August 11, 2023 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
| August 3, 2020 | NAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
Other documents for ABS Corporation
- FDA Inspection 1298654 - 2026-01-16
- FDA Inspection 1269360 - 2025-04-29
- FDA Inspection 1248321 - 2024-08-13
- FDA Inspection 1215124 - 2023-08-11
- FDA Inspection 1127879 - 2020-08-03
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