FDA Inspection
LPT Laboratory of Pharmacology and Toxicology GmbH & Co. KGLPT Laboratory of Pharmacology and Toxicology GmbH & Co. KG – FDA Inspection, Jun 28, 2018
Record Details
This FDA Inspection record concerns LPT Laboratory of Pharmacology and Toxicology GmbH & Co. KG, with an inspection on June 28, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- June 28, 2018
- Product Type
- Drugs
View Company Profile
ID · f0f57c87-6c22-4169-8015-1ee746433dde
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1060026
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of LPT Laboratory of Pharmacology and Toxicology GmbH & Co. KG
2| Date | Classification | Office | Project area |
|---|---|---|---|
| June 19, 2015 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 3, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for LPT Laboratory of Pharmacology and Toxicology GmbH & Co. KG
- FDA Inspection 945371 - 2015-06-19
- FDA Inspection 770067 - 2012-02-03
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.