FDA Inspection
Renaissance Lakewood, LLCRenaissance Lakewood, LLC – FDA Inspection, Aug 22, 2019
Record Details
This FDA Inspection record concerns Renaissance Lakewood, LLC, with an inspection on August 22, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
View Company Profile
ID · 1926619d-ccab-483b-a3a3-928861282710
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1100331
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Renaissance Lakewood, LLC
13| Date | Classification | Office | Project area |
|---|---|---|---|
| July 29, 2026 | Not classified | New Jersey District Office | Drug Quality Assurance |
| June 6, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 15, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 26, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 1, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Renaissance Lakewood, LLC
- FDA Inspection 1327338 - 2026-07-29
- FDA Inspection 1209603 - 2023-06-06
- FDA Inspection 1045720 - 2018-03-15
- FDA Inspection 1009890 - 2017-04-26
- FDA Inspection 973346 - 2016-06-01
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.