FDA Inspection
OPMX, LLCFDA Inspection 726123 - OPMX, LLC - May 31, 2011
Record Details
This FDA Inspection record concerns OPMX, LLC, with an inspection on May 31, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- OPMX, LLC
- Inspection Date
- May 31, 2011
- Product Type
- Drugs
View Company Profile
ID · 82776e4d-5e62-45cf-9957-a913731a6d1d
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 726123
- FDA center
- Human Drugs
- Project area
- Unapproved and Misbranded Drugs
FDA Citations
3- 21 CFR 111.70(d)Specifications - labels, packaging
- 21 CFR 111.153Written procedures - labels
- 21 CFR 111.120Quality control operations - components, packaging, labels
Full citation text and observation details available on the Dashboard.
Other FDA inspections of OPMX, LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| September 24, 2026 | NAI | Center for Food Safety and Applied Nutrition | Foodborne Biological Hazards |
| December 10, 2024 | Not classified | Los Angeles District Office | |
| July 7, 2023 | VAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
| February 20, 2013 | NAI | Center for Drug Evaluation and Research | Unapproved and Misbranded Drugs |
Other documents for OPMX, LLC
- FDA Inspection 1337610 - 2026-09-24
- FDA Inspection 1256972 - 2024-12-10
- FDA Inspection 1209844 - 2023-07-07
- FDA Inspection 820229 - 2013-02-20
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