FDA Inspection
ActiTech, LPActiTech, LP – FDA Inspection, May 24, 2010
Record Details
This FDA Inspection record concerns ActiTech, LP, with an inspection on May 24, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- ActiTech, LP
- Inspection Date
- May 24, 2010
- Product Type
- Drugs
View Company Profile
ID · 628956ea-d5bb-45f1-a865-01707e7ba1b6
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 663582
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.160(a)Deviations from laboratory control requirements
- 21 CFR 211.180(e)Records reviewed annually
- 21 CFR 211.100(a)Absence of Written Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of ActiTech, LP
3| Date | Classification | Office | Project area |
|---|---|---|---|
| September 25, 2019 | NAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
| August 23, 2011 | NAI | Center for Food Safety and Applied Nutrition | Colors and Cosmetics Technology |
| March 13, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for ActiTech, LP
- FDA Inspection 1105208 - 2019-09-25
- FDA Inspection 749662 - 2011-08-23
- FDA Inspection 570526 - 2009-03-13
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.