FDA Inspection
Ohm Laboratories Inc.Ohm Laboratories Inc. – FDA Inspection, Dec 18, 2012
Record Details
This FDA Inspection record concerns Ohm Laboratories Inc., with an inspection on December 18, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Ohm Laboratories Inc.
- Inspection Date
- December 18, 2012
- Product Type
- Drugs
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ID · 2d0b892b-a3e2-41ee-9a87-16438e3723f0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 812095
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.84(b)Representative Samples
- 21 CFR 211.192Investigations of discrepancies, failures
- 21 CFR 211.100(b)SOPs not followed / documented
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Other FDA inspections of Ohm Laboratories Inc.
23| Date | Classification | Office | Project area |
|---|---|---|---|
| October 31, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 12, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 16, 2023 | Not classified | New Jersey District Office | |
| November 10, 2022 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 2, 2021 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Ohm Laboratories Inc.
- FDA Inspection 1254992 - 2024-10-31
- FDA Inspection 1230728 - 2024-01-12
- FDA Inspection 1207376 - 2023-05-16
- FDA Inspection 1192906 - 2022-11-10
- FDA Inspection 1151837 - 2021-08-02
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