Nancy L. Rolli
FDA investigator
Appears on 4 documents from 2005 to 2015, mostly at sites in New Jersey. Most often cites production record review (21 CFR 211.192).
- 4
- Documents on file
- 8.3
- Observations per 483
- 2005
- First seen
- 2015
- Most recent
What they cite most
From 25 observations- 21 CFR 211.192Production record review5
- 21 CFR 211.22Responsibilities of quality control unit4
- 21 CFR 314.81Other postmarketing reports3
- 21 CFR 211.160General requirements2
- 21 CFR 211.165Testing and release for distribution2
- 21 CFR 211.194Laboratory records2
Activity by year
2005: 2, 2006: 1, 2015: 1
Where
New Jersey 4
Often inspects with
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Inspection history
4 documents, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2015-07-24 | Amended 483 Able Laboratories, Inc.Jul 24, 2015 · Cranbury, New Jersey | Cranbury, New Jersey | 1 | |
| 2006-08-10 | EIR Actavis Totowa LLCAug 10, 2006 · Little Falls, New Jersey | Little Falls, New Jersey | — | |
| 2005-07-06 | Amended 483 Able Laboratories, Inc.Jul 6, 2005 · Cranbury, New Jersey | Cranbury, New Jersey | 12 | |
| 2005-07-01 | 483 Able Laboratories, IncJul 1, 2005 · Cranbury, New Jersey | Cranbury, New Jersey | 12 |
About this profile
What does Nancy L. Rolli inspect?
Nancy L. Rolli appears on 4 documents on file covering 2 sites, mostly in New Jersey.
What do they cite most often?
21 CFR 211.192 (production record review), followed by 21 CFR 211.22 and 21 CFR 314.81.
Can I read the observations?
Each document page previews the opening words of every observation. The full documents are available to buy, one at a time or together.
How current is this profile?
The most recent document on file for Nancy L. Rolli is dated Jul 24, 2015.