FDA Inspection
Lornamead Inc.Lornamead Inc. – FDA Inspection, May 7, 2010
Record Details
This FDA Inspection record concerns Lornamead Inc., with an inspection on May 7, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Lornamead Inc.
- Inspection Date
- May 7, 2010
- Product Type
- Drugs
View Company Profile
ID · a322ea6f-0972-47aa-8568-2aa333567678
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 662789
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.194(a)Complete test data included in records
- 21 CFR 211.166(a)Written program not followed
- 21 CFR 211.192Written record of investigation incomplete
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Lornamead Inc.
7| Date | Classification | Office | Project area |
|---|---|---|---|
| January 21, 2026 | VAI | New York District Office | Drug Quality Assurance |
| June 5, 2025 | Not classified | New York District Office | |
| April 11, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 18, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 7, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Lornamead Inc.
- FDA Inspection 1299288 - 2026-01-21
- FDA Inspection 1263485 - 2025-06-05
- FDA Inspection 1202257 - 2023-04-11
- FDA Inspection 955642 - 2015-12-18
- FDA Inspection 836243 - 2013-06-07
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.